Variant report

Variant	nsv456466
Chromosome Location	chr14:105615648-105685865
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2727)
CpG islands
(count:4579)
Chromatin interactive
region (count:190)
LncRNA
region (count:4)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2727 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105635551-105635751	K562	blood:	n/a	n/a
2	ARID3A	chr14:105646970-105647099	K562	blood:	n/a	n/a
3	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
4	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
5	ATF3	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
6	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
7	ATF3	chr14:105665582-105665772	K562	blood:	n/a	n/a
8	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:105669384-105669662	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr14:105662435-105662753	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr14:105663077-105663199	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr14:105668932-105669779	A549	lung:	n/a	n/a
16	BCL3	chr14:105670617-105671440	A549	lung:	n/a	n/a
17	BCL3	chr14:105681677-105681921	GM12878	blood:	n/a	n/a
18	BCL3	chr14:105681691-105682038	GM12878	blood:	n/a	n/a
19	BCL3	chr14:105667847-105668627	A549	lung:	n/a	chr14:105667887-105667896 chr14:105668189-105668198 chr14:105667888-105667897
20	BCL3	chr14:105668099-105668659	A549	lung:	n/a	chr14:105668189-105668198
21	BCL3	chr14:105669015-105669647	A549	lung:	n/a	n/a
22	BHLHE40	chr14:105673381-105673508	K562	blood:	n/a	n/a
23	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
24	BHLHE40	chr14:105670862-105671194	HepG2	liver:	n/a	n/a
25	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
26	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
27	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
28	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
29	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
30	BRCA1	chr14:105663594-105663903	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
32	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
33	CBX3	chr14:105665434-105665804	K562	blood:	n/a	n/a
34	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
35	CCNT2	chr14:105673513-105673600	K562	blood:	n/a	n/a
36	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
37	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
38	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
39	CCNT2	chr14:105665556-105665715	K562	blood:	n/a	n/a
40	CCNT2	chr14:105662979-105663291	K562	blood:	n/a	n/a
41	CCNT2	chr14:105672167-105672351	K562	blood:	n/a	n/a
42	CEBPB	chr14:105669556-105669564	HepG2	liver:	n/a	n/a
43	CEBPB	chr14:105646836-105646884	K562	blood:	n/a	n/a
44	CEBPB	chr14:105663593-105663880	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr14:105671141-105671144	Hela-S3	cervix:	n/a	n/a
47	CHD1	chr14:105673884-105674043	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr14:105635288-105635741	K562	blood:	n/a	n/a
49	CHD2	chr14:105647556-105647857	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a

(count:4579 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105683798-105683848	LNCaP	prostate:	n/a
2	chr14:105669480-105669530	NB4	blood:	n/a
3	chr14:105660876-105660926	ECC-1	luminal epithelium:	n/a
4	chr14:105648697-105648747	H1-hESC	embryonic stem cell:	embryo
5	chr14:105683798-105683848	LNCaP	prostate:	n/a
6	chr14:105669480-105669530	NB4	blood:	n/a
7	chr14:105660876-105660926	ECC-1	luminal epithelium:	n/a
8	chr14:105648697-105648747	H1-hESC	embryonic stem cell:	embryo
9	chr14:105685021-105685071	HAEpiC	amniotic membrane:	n/a
10	chr14:105618482-105618532	NH-A	brain:	n/a
11	chr14:105685075-105685125	HCPEpiC	choroid plexus:	n/a
12	chr14:105634387-105634437	NHDF-neo	bronchial:	n/a
13	chr14:105685616-105685666	NB4	blood:	n/a
14	chr14:105622992-105623042	HNPCEpiC	eye:	n/a
15	chr14:105662787-105662837	MCF-7	breast:	n/a
16	chr14:105619511-105619561	GM12891	blood:	n/a
17	chr14:105635208-105635258	AG04450	lung:	fetal
18	chr14:105685075-105685125	PFSK-1	brain:	n/a
19	chr14:105635208-105635258	Caco-2	colon:	n/a
20	chr14:105647407-105647457	NH-A	brain:	n/a
21	chr14:105648024-105648074	ProgFib	skin:	n/a
22	chr14:105619701-105619751	RPTEC	kidney:	n/a
23	chr14:105685732-105685782	HIPEpiC	eye:	n/a
24	chr14:105649097-105649147	ovcar-3	ovarian:	n/a
25	chr14:105659225-105659275	HMEC	breast:	n/a
26	chr14:105658685-105658735	SK-N-SH_RA	brain:	n/a
27	chr14:105651786-105651836	HEEpiC	esophagus:	n/a
28	chr14:105648224-105648274	AG09319	gingival:	n/a
29	chr14:105659225-105659275	T-47D	breast:	n/a
30	chr14:105681416-105681466	AG09309	skin:	n/a
31	chr14:105685616-105685666	SK-N-SH_RA	brain:	n/a
32	chr14:105676908-105676958	GM12891	blood:	n/a
33	chr14:105617575-105617625	NH-A	brain:	n/a
34	chr14:105635706-105635756	ECC-1	luminal epithelium:	n/a
35	chr14:105616988-105617038	AG04449	skin:	fetal
36	chr14:105624483-105624533	Jurkat	blood:	n/a
37	chr14:105655398-105655448	NB4	blood:	n/a
38	chr14:105667508-105667558	HRPEpiC	eye:	n/a
39	chr14:105676846-105676896	GM06990	blood:	n/a
40	chr14:105622454-105622504	HCT-116	colon:	n/a
41	chr14:105617308-105617358	HL-60	blood:	n/a
42	chr14:105639304-105639354	BJ	skin:	n/a
43	chr14:105647407-105647457	NT2-D1	testis:	n/a
44	chr14:105635236-105635286	A549	lung:	n/a
45	chr14:105655178-105655228	NHDF-neo	bronchial:	n/a
46	chr14:105635708-105635758	Hepatocyte	liver:	n/a
47	chr14:105647510-105647560	PANC-1	pancreas:	n/a
48	chr14:105685660-105685710	HEK293	kidney:	embryo
49	chr14:105684005-105684055	GM12892	blood:	n/a
50	chr14:105683925-105683975	AoSMC	blood vessel:	n/a

(count:190 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:105671811..105674041-chr14:105933944..105936633,2	MCF-7	breast:
2	chr14:105550862..105553369-chr14:105650448..105653112,3	MCF-7	breast:
3	chr14:105559890..105560867-chr14:105633779..105634301,2	MCF-7	breast:
4	chr14:105646294..105648744-chr14:105860219..105862499,2	MCF-7	breast:
5	chr14:105637173..105640162-chr14:105646187..105648550,3	MCF-7	breast:
6	chr14:105665489..105668109-chr14:105740976..105743490,2	MCF-7	breast:
7	chr14:105650402..105652151-chr14:105657349..105659937,3	MCF-7	breast:
8	chr14:105669618..105672409-chr14:105805481..105807820,2	K562	blood:
9	chr14:105512170..105512763-chr14:105653793..105654556,2	MCF-7	breast:
10	chr14:105645461..105647244-chr14:105649629..105652172,2	MCF-7	breast:
11	chr14:105668328..105670868-chr14:105672731..105674371,2	MCF-7	breast:
12	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
13	chr14:105670331..105671987-chr14:105672268..105674643,2	K562	blood:
14	chr14:105667147..105672450-chr14:105672961..105678949,7	MCF-7	breast:
15	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:
16	chr14:105568093..105570383-chr14:105666909..105669878,2	K562	blood:
17	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
18	chr14:105611629..105615687-chr14:105625576..105630230,4	K562	blood:
19	chr14:105650402..105652151-chr14:105657349..105659937,3	MCF-7	breast:
20	chr14:105669002..105670184-chr14:105747515..105748746,6	MCF-7	breast:
21	chr14:105634303..105636398-chr14:105650780..105653428,2	MCF-7	breast:
22	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
23	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:
24	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
25	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
26	chr14:105646332..105648438-chr14:105653932..105656621,2	K562	blood:
27	chr14:105647532..105649524-chr14:105654465..105656702,2	MCF-7	breast:
28	chr14:105642956..105644640-chr14:105647161..105649743,2	MCF-7	breast:
29	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
30	chr14:105486956..105489375-chr14:105652100..105655755,4	MCF-7	breast:
31	chr14:105669972..105673331-chr14:105732479..105735063,3	MCF-7	breast:
32	chr14:105502174..105504922-chr14:105632204..105633983,2	MCF-7	breast:
33	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
34	chr14:105647951..105651045-chr14:105657056..105659475,3	MCF-7	breast:
35	chr14:105667874..105671061-chr14:105780211..105783022,3	K562	blood:
36	chr14:105556509..105557265-chr14:105631240..105632200,2	MCF-7	breast:
37	chr14:105636897..105638962-chr14:105660422..105663007,2	MCF-7	breast:
38	chr14:105668316..105670026-chr14:105722977..105725479,2	MCF-7	breast:
39	chr14:105647877..105649605-chr14:105663025..105665566,2	MCF-7	breast:
40	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:
41	chr14:105556528..105557420-chr14:105633531..105634669,3	MCF-7	breast:
42	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
43	chr14:105667141..105669666-chr14:105676688..105678333,2	K562	blood:
44	chr14:105668328..105670868-chr14:105672731..105674371,2	MCF-7	breast:
45	chr14:105450462..105452951-chr14:105633617..105637647,3	MCF-7	breast:
46	chr14:105667435..105668434-chr14:105747893..105748852,3	MCF-7	breast:
47	chr14:105680829..105682565-chr14:105686561..105688543,2	MCF-7	breast:
48	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
49	chr14:105668621..105671368-chr14:105688558..105691360,2	K562	blood:
50	chr14:105669895..105672499-chr14:105780191..105782899,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1
2	lnc-BTBD6-3	chr14:105681490-105682260	NONHSAT040337
3	lnc-BTBD6-3	chr14:105682370-105682401	NONHSAT040337
4	lnc-BTBD6-1	chr14:105639541-105639584	ENSG00000257816.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431

No data

Variant related genes	Relation type
JAG2	TF binding region
BRF1	TF binding region
ENSG00000257622	TF binding region
NUDT14	TF binding region
JAG2	CpG island
BRF1	CpG island
ENSG00000257622	CpG island
NUDT14	CpG island
ENSG00000140104	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000256498	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000170027	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000182979	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000185567	chromatin interactions

Extended variants
information (count: 2992 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2992 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9972231	chr14:105615648-105615649	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587692038	chr14:105615649-105615650	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs181385226	chr14:105615664-105615665	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587637403	chr14:105615675-105615676	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375265020	chr14:105615678-105615679	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs201695814	chr14:105615696-105615697	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs373693762	chr14:105615705-105615706	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs587601994	chr14:105615715-105615716	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs587636118	chr14:105615733-105615734	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs150065796	chr14:105615763-105615764	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs587615094	chr14:105615823-105615824	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs587695083	chr14:105615840-105615841	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs145393197	chr14:105615854-105615855	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs148771502	chr14:105615867-105615868	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs587659509	chr14:105615896-105615897	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs587745527	chr14:105615919-105615920	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs149319748	chr14:105616009-105616010	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs587613158	chr14:105616034-105616035	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs57311278	chr14:105616093-105616094	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs587703980	chr14:105616095-105616096	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs587738803	chr14:105616122-105616123	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs587691753	chr14:105616123-105616124	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs587746422	chr14:105616124-105616125	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs587627788	chr14:105616148-105616149	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs587674727	chr14:105616161-105616162	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587761287	chr14:105616225-105616226	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs61501482	chr14:105616281-105616282	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs587646913	chr14:105616285-105616286	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs59841145	chr14:105616291-105616292	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs587633202	chr14:105616292-105616293	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs57747467	chr14:105616294-105616295	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs61064371	chr14:105616333-105616334	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs57501244	chr14:105616337-105616338	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs184755905	chr14:105616349-105616350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs587741852	chr14:105616457-105616458	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587771495	chr14:105616489-105616490	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs142383191	chr14:105616522-105616523	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs587731748	chr14:105616531-105616532	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs72707615	chr14:105616558-105616559	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373497554	chr14:105616647-105616648	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs587664624	chr14:105616693-105616694	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs587716127	chr14:105616699-105616700	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs587604290	chr14:105616717-105616718	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs370702806	chr14:105616768-105616769	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587736791	chr14:105616780-105616781	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs189209081	chr14:105616856-105616857	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs59700762	chr14:105616870-105616871	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs369995305	chr14:105616885-105616886	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587729034	chr14:105616947-105616948	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs180968250	chr14:105616956-105616957	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:2927 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105602800-105629800	Weak transcription	K562	blood
2	chr14:105606400-105617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
3	chr14:105606800-105618000	Weak transcription	Psoas Muscle	Psoas
4	chr14:105606800-105619600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
6	chr14:105607000-105618200	Strong transcription	Gastric	stomach
7	chr14:105607000-105621600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr14:105607200-105616000	Strong transcription	HMEC	breast
9	chr14:105607200-105619600	Weak transcription	Colonic Mucosa	Colon
10	chr14:105607400-105619200	Strong transcription	Pancreas	Pancrea
11	chr14:105607600-105616000	Strong transcription	Fetal Intestine Small	intestine
12	chr14:105607600-105617600	Strong transcription	Skeletal Muscle Male	skeletal muscle
13	chr14:105607600-105625400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:105607600-105632000	Weak transcription	Brain Angular Gyrus	brain
15	chr14:105608000-105618000	Strong transcription	Adipose Nuclei	Adipose
16	chr14:105608200-105616400	Strong transcription	Right Ventricle	heart
17	chr14:105608800-105618400	Strong transcription	Lung	lung
18	chr14:105609400-105631400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr14:105609600-105618800	Weak transcription	Placenta	Placenta
20	chr14:105609600-105622000	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr14:105610000-105631400	Weak transcription	HUVEC	blood vessel
22	chr14:105610200-105625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:105611200-105615800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
24	chr14:105611800-105616000	Strong transcription	NHEK	skin
25	chr14:105612000-105615800	Strong transcription	Left Ventricle	heart
26	chr14:105612800-105621000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr14:105613400-105623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr14:105613400-105631400	Weak transcription	Brain Anterior Caudate	brain
29	chr14:105613600-105618400	Weak transcription	HSMMtube	muscle
30	chr14:105613600-105619200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr14:105613600-105631400	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr14:105613800-105615800	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr14:105613800-105616600	Weak transcription	Brain Germinal Matrix	brain
34	chr14:105613800-105616600	Weak transcription	Fetal Muscle Trunk	muscle
35	chr14:105613800-105631400	Weak transcription	Brain Cingulate Gyrus	brain
36	chr14:105614000-105620200	Weak transcription	Fetal Brain Female	brain
37	chr14:105614000-105621600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:105614000-105622000	Weak transcription	Brain Hippocampus Middle	brain
39	chr14:105614600-105616000	Genic enhancers	Spleen	Spleen
40	chr14:105614600-105619000	Strong transcription	Fetal Stomach	stomach
41	chr14:105614800-105616800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr14:105615200-105616000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr14:105615200-105621600	Weak transcription	Esophagus	oesophagus
44	chr14:105615200-105625600	Weak transcription	A549	lung
45	chr14:105615400-105616200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:105615600-105615800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr14:105615600-105616600	Weak transcription	Fetal Muscle Leg	muscle
48	chr14:105615600-105616800	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr14:105615800-105616000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr14:105615800-105616200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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