Variant report

Variant	nsv5524
Chromosome Location	chr6:147428436-147454371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:142)
CpG islands
(count:61)
Chromatin interactive
region (count:35)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:142 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:147448955-147449227	K562	blood:	n/a	chr6:147449136-147449152
2	ARID3A	chr6:147448044-147448261	K562	blood:	n/a	n/a
3	ATF1	chr6:147447930-147448233	K562	blood:	n/a	n/a
4	ATF1	chr6:147453906-147454448	K562	blood:	n/a	n/a
5	ATF1	chr6:147452950-147453307	K562	blood:	n/a	n/a
6	ATF3	chr6:147453890-147454437	K562	blood:	n/a	n/a
7	BHLHE40	chr6:147447867-147448241	K562	blood:	n/a	n/a
8	CCNT2	chr6:147454071-147454077	K562	blood:	n/a	n/a
9	CEBPB	chr6:147454053-147454490	HepG2	liver:	n/a	chr6:147454311-147454322
10	CEBPB	chr6:147428152-147428477	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr6:147452987-147453291	HepG2	liver:	n/a	chr6:147453112-147453123
12	CEBPB	chr6:147454185-147454433	K562	blood:	n/a	chr6:147454311-147454322
13	CEBPB	chr6:147454017-147454499	IMR90	lung:	n/a	chr6:147454311-147454322
14	CEBPB	chr6:147452985-147453238	K562	blood:	n/a	chr6:147453112-147453123
15	CEBPB	chr6:147454153-147454448	A549	lung:	n/a	chr6:147454311-147454322
16	CEBPB	chr6:147440505-147440819	K562	blood:	n/a	chr6:147440639-147440650
17	CEBPB	chr6:147440467-147440831	HepG2	liver:	n/a	chr6:147440639-147440650
18	CEBPB	chr6:147428151-147428520	K562	blood:	n/a	n/a
19	CEBPB	chr6:147453973-147454514	K562	blood:	n/a	chr6:147454311-147454322
20	CEBPB	chr6:147452942-147453288	IMR90	lung:	n/a	chr6:147453112-147453123
21	CEBPB	chr6:147454028-147454480	H1-hESC	embryonic stem cell:	n/a	chr6:147454311-147454322
22	CEBPB	chr6:147440482-147440806	A549	lung:	n/a	chr6:147440639-147440650
23	CEBPB	chr6:147452961-147453288	A549	lung:	n/a	chr6:147453112-147453123
24	CEBPB	chr6:147452943-147453296	Hela-S3	cervix:	n/a	chr6:147453112-147453123
25	CEBPB	chr6:147453935-147454500	K562	blood:	n/a	chr6:147454311-147454322
26	CEBPB	chr6:147454084-147454505	Hela-S3	cervix:	n/a	chr6:147454311-147454322
27	CEBPB	chr6:147428123-147428528	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:147428107-147428473	K562	blood:	n/a	n/a
29	CEBPB	chr6:147454129-147454462	ECC-1	luminal epithelium:	n/a	chr6:147454311-147454322
30	CEBPB	chr6:147452982-147453266	H1-hESC	embryonic stem cell:	n/a	chr6:147453112-147453123
31	CEBPB	chr6:147428148-147428494	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:147428152-147428450	A549	lung:	n/a	n/a
33	CEBPB	chr6:147452919-147453311	K562	blood:	n/a	chr6:147453112-147453123
34	CEBPB	chr6:147428219-147428500	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:147452896-147453356	K562	blood:	n/a	chr6:147453112-147453123
36	CEBPB	chr6:147454157-147454495	ECC-1	luminal epithelium:	n/a	chr6:147454311-147454322
37	CEBPB	chr6:147440484-147440794	IMR90	lung:	n/a	chr6:147440639-147440650
38	CTCF	chr6:147446632-147446650	GM20000	blood:	n/a	n/a
39	CTCF	chr6:147452940-147453090	AG10803	skin:	n/a	n/a
40	CTCF	chr6:147438860-147439010	BJ	skin:	n/a	n/a
41	CUX1	chr6:147428264-147428809	K562	blood:	n/a	n/a
42	CUX1	chr6:147447542-147448066	K562	blood:	n/a	n/a
43	CUX1	chr6:147454259-147454267	K562	blood:	n/a	n/a
44	E2F4	chr6:147432968-147433212	MCF10A-Er-Src	breast:	n/a	n/a
45	EBF1	chr6:147438687-147439012	GM12878	blood:	n/a	chr6:147438853-147438863 chr6:147438852-147438863 chr6:147438853-147438862
46	EP300	chr6:147447886-147448255	K562	blood:	n/a	n/a
47	EP300	chr6:147454260-147454502	Hela-S3	cervix:	n/a	chr6:147454312-147454326
48	EP300	chr6:147453098-147453197	K562	blood:	n/a	n/a
49	EP300	chr6:147453883-147454410	K562	blood:	n/a	chr6:147454312-147454326
50	EP300	chr6:147428228-147428437	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147428486-147428536	HEEpiC	esophagus:	n/a
2	chr6:147428486-147428536	HNPCEpiC	eye:	n/a
3	chr6:147428486-147428536	NH-A	brain:	n/a
4	chr6:147428486-147428536	NHDF-neo	bronchial:	n/a
5	chr6:147428486-147428536	HEK293	kidney:	embryo
6	chr6:147428486-147428536	Hepatocyte	liver:	n/a
7	chr6:147428486-147428536	H1-hESC	embryonic stem cell:	embryo
8	chr6:147428486-147428536	HRCEpiC	kidney:	n/a
9	chr6:147428486-147428536	CMK	blood:	n/a
10	chr6:147428486-147428536	A549	lung:	n/a
11	chr6:147428486-147428536	Caco-2	colon:	n/a
12	chr6:147428486-147428536	IMR90	lung:	fetal
13	chr6:147428486-147428536	HCM	heart:	n/a
14	chr6:147428486-147428536	HCF	heart:	n/a
15	chr6:147428486-147428536	SKMC	muscle:	n/a
16	chr6:147428486-147428536	ProgFib	skin:	n/a
17	chr6:147428486-147428536	NB4	blood:	n/a
18	chr6:147428486-147428536	MCF-7	breast:	n/a
19	chr6:147428486-147428536	GM12878	blood:	n/a
20	chr6:147428486-147428536	Jurkat	blood:	n/a
21	chr6:147428486-147428536	HRE	kidney:	n/a
22	chr6:147428486-147428536	GM06990	blood:	n/a
23	chr6:147428486-147428536	HPAEpiC	pulmonary alveolar:	n/a
24	chr6:147428486-147428536	NHBE	bronchial:	n/a
25	chr6:147428486-147428536	PrEC	prostate:	n/a
26	chr6:147428486-147428536	SK-N-SH	brain:	n/a
27	chr6:147428486-147428536	HRPEpiC	eye:	n/a
28	chr6:147428486-147428536	HAEpiC	amniotic membrane:	n/a
29	chr6:147428486-147428536	GM12891	blood:	n/a
30	chr6:147428486-147428536	RPTEC	kidney:	n/a
31	chr6:147428486-147428536	SAEC	small airway:	n/a
32	chr6:147428486-147428536	AG10803	skin:	n/a
33	chr6:147428486-147428536	NT2-D1	testis:	n/a
34	chr6:147428486-147428536	PANC-1	pancreas:	n/a
35	chr6:147428486-147428536	HIPEpiC	eye:	n/a
36	chr6:147428486-147428536	BE2_C	brain:	n/a
37	chr6:147428486-147428536	BJ	skin:	n/a
38	chr6:147428486-147428536	GM12892	blood:	n/a
39	chr6:147428486-147428536	HMEC	breast:	n/a
40	chr6:147428486-147428536	LNCaP	prostate:	n/a
41	chr6:147428486-147428536	PFSK-1	brain:	n/a
42	chr6:147428486-147428536	AG09309	skin:	n/a
43	chr6:147428486-147428536	AG04449	skin:	fetal
44	chr6:147428486-147428536	AoSMC	blood vessel:	n/a
45	chr6:147428486-147428536	HCT-116	colon:	n/a
46	chr6:147428486-147428536	K562	blood:	n/a
47	chr6:147428486-147428536	HUVEC	blood vessel:	n/a
48	chr6:147428486-147428536	SK-N-MC	brain:	n/a
49	chr6:147428486-147428536	AG04450	lung:	fetal
50	chr6:147428486-147428536	Hela-S3	cervix:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:147442873..147445423-chr6:147447092..147450084,3	K562	blood:
2	chr6:147427313..147429430-chr6:147435405..147437072,2	K562	blood:
3	chr6:147449104..147452134-chr6:147521705..147524376,3	K562	blood:
4	chr6:147450846..147453025-chr6:147455330..147456851,2	K562	blood:
5	chr6:147448469..147450107-chr6:147480618..147482536,2	K562	blood:
6	chr6:147437032..147439799-chr6:147479756..147483330,3	K562	blood:
7	chr6:147420000..147421600-chr6:147444950..147446900,2	K562	blood:
8	chr6:147436472..147438342-chr6:147524210..147525806,2	K562	blood:
9	chr6:147425896..147428449-chr6:147432490..147434531,2	K562	blood:
10	chr6:147443197..147445695-chr6:147447092..147449198,3	K562	blood:
11	chr6:147206418..147208548-chr6:147443169..147444927,2	K562	blood:
12	chr6:147232453..147234855-chr6:147426627..147429327,2	K562	blood:
13	chr6:147431206..147434248-chr6:147448632..147451102,3	K562	blood:
14	chr6:147408861..147411040-chr6:147429825..147431994,2	MCF-7	breast:
15	chr6:147205707..147208071-chr6:147446110..147448975,2	K562	blood:
16	chr6:147426207..147429085-chr6:147439279..147441613,3	K562	blood:
17	chr6:147450226..147452733-chr6:147453592..147455134,2	MCF-7	breast:
18	chr6:147450226..147452733-chr6:147453592..147455134,2	MCF-7	breast:
19	chr6:147439196..147441349-chr6:147442627..147444720,2	K562	blood:
20	chr6:147424959..147428934-chr6:147429472..147432018,4	MCF-7	breast:
21	chr6:147431206..147434248-chr6:147448632..147451102,3	K562	blood:
22	chr6:147454119..147456933-chr6:147477861..147480399,2	K562	blood:
23	chr6:147444618..147450604-chr6:147522868..147525613,5	K562	blood:
24	chr6:147425896..147428449-chr6:147432490..147434531,2	K562	blood:
25	chr6:147424959..147428934-chr6:147429472..147432018,4	MCF-7	breast:
26	chr6:147426845..147428573-chr6:147517289..147519124,2	K562	blood:
27	chr6:147443197..147445695-chr6:147447092..147449198,3	K562	blood:
28	chr6:147420322..147423479-chr6:147424445..147428438,5	K562	blood:
29	chr6:147427313..147429430-chr6:147435405..147437072,2	K562	blood:
30	chr6:147444618..147448915-chr6:147522478..147526449,6	K562	blood:
31	chr6:147446688..147448546-chr6:147474498..147476010,2	K562	blood:
32	chr6:147442930..147446294-chr6:147532679..147536475,3	K562	blood:
33	chr6:147450043..147452990-chr6:147474130..147476017,2	K562	blood:
34	chr6:147430213..147433528-chr6:147478461..147482182,3	K562	blood:
35	chr6:147442873..147445423-chr6:147447092..147450084,3	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHPRH-2	chr6:147440553-147440613	NONHSAT115441
2	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
3	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
4	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
5	lnc-SHPRH-2	chr6:147440553-147440613	NONHSAT115433
6	lnc-SHPRH-2	chr6:147453002-147453054	ENSG00000233452
7	lnc-SHPRH-2	chr6:147453002-147453122	NONHSAT115441
8	lnc-SHPRH-2	chr6:147440553-147440613	ENSG00000233452
9	lnc-SHPRH-2	chr6:147453002-147453122	ENSG00000233452
10	lnc-SHPRH-2	chr6:147440553-147440599	ENSG00000233452

No data

Variant related genes	Relation type
STXBP5-AS1	TF binding region
STXBP5-AS1	CpG island
ENSG00000164506	chromatin interactions
ENSG00000233452	chromatin interactions
ENSG00000196634	chromatin interactions
PPP1CB	miRNA target sites
RBMX	miRNA target sites
MTMR4	miRNA target sites
ADAM12	miRNA target sites
PPP1R13B	miRNA target sites
HAND1	miRNA target sites
TMEM161B	miRNA target sites

Extended variants
information (count: 863 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113568545	chr6:147428506-147428507	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs76735927	chr6:147428520-147428521	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555275585	chr6:147428530-147428531	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575091325	chr6:147428580-147428581	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543995188	chr6:147428595-147428596	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563863722	chr6:147428596-147428597	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs6919676	chr6:147428635-147428636	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566022636	chr6:147428693-147428694	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374401202	chr6:147428698-147428699	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73786896	chr6:147428707-147428708	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534806339	chr6:147428757-147428758	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192961189	chr6:147428765-147428766	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73574485	chr6:147428809-147428810	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs560809011	chr6:147428837-147428838	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548148388	chr6:147428859-147428860	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529928152	chr6:147428865-147428866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs184673693	chr6:147428889-147428890	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569489152	chr6:147428942-147428943	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147267355	chr6:147428950-147428951	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371632502	chr6:147428958-147428959	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568126710	chr6:147428962-147428963	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552604488	chr6:147428994-147428995	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs565964510	chr6:147429015-147429016	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534972577	chr6:147429034-147429035	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73786898	chr6:147429039-147429040	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs188253074	chr6:147429074-147429075	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs376336474	chr6:147429200-147429201	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78885112	chr6:147429213-147429214	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371719632	chr6:147429219-147429220	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs544793390	chr6:147429221-147429222	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6920901	chr6:147429298-147429299	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs552237773	chr6:147429317-147429318	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571954690	chr6:147429324-147429325	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540666045	chr6:147429326-147429327	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191259891	chr6:147429331-147429332	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs538441985	chr6:147429339-147429340	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs116903753	chr6:147429379-147429380	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs184839603	chr6:147429388-147429389	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs75716875	chr6:147429403-147429404	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs575121733	chr6:147429426-147429427	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs552396007	chr6:147429433-147429434	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377411489	chr6:147429493-147429494	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs534801845	chr6:147429539-147429540	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs189353426	chr6:147429567-147429568	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs151240305	chr6:147429569-147429570	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs140446854	chr6:147429575-147429576	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs181727411	chr6:147429622-147429623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs117592615	chr6:147429632-147429633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539980991	chr6:147429658-147429659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149946584	chr6:147429662-147429663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147424800-147429400	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr6:147425200-147429800	Weak transcription	Fetal Thymus	thymus
3	chr6:147425200-147430600	Weak transcription	Dnd41	blood
4	chr6:147425800-147429600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr6:147425800-147430000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:147427800-147428800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:147427800-147428800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr6:147427800-147428800	Enhancers	NHDF-Ad	bronchial
9	chr6:147427800-147429000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:147428000-147428600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:147428000-147428600	Flanking Active TSS	Osteobl	bone
12	chr6:147428000-147428800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr6:147428000-147428800	Enhancers	HepG2	liver
14	chr6:147428000-147429000	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr6:147428000-147430600	Enhancers	Primary T cells from cord blood	blood
16	chr6:147428000-147430800	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr6:147428000-147431000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr6:147428000-147431000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr6:147428000-147431800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr6:147428200-147428600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:147428200-147428600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
22	chr6:147428200-147428600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr6:147428200-147428600	Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr6:147428200-147428600	Flanking Active TSS	K562	blood
25	chr6:147428200-147428800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:147428200-147430600	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr6:147428200-147430600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
28	chr6:147428400-147428600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:147428400-147428600	Enhancers	Liver	Liver
30	chr6:147428400-147428600	Flanking Active TSS	NHLF	lung
31	chr6:147428400-147428800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:147428400-147429400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr6:147428600-147428800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:147428600-147428800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr6:147428600-147428800	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr6:147428600-147428800	Flanking Active TSS	Liver	Liver
37	chr6:147428600-147428800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
38	chr6:147428600-147428800	Enhancers	NHLF	lung
39	chr6:147428600-147428800	Enhancers	Osteobl	bone
40	chr6:147428600-147431000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr6:147428800-147429000	Enhancers	Liver	Liver
42	chr6:147428800-147429200	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr6:147429000-147429400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr6:147429000-147429400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr6:147429200-147429400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr6:147429400-147429600	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr6:147429400-147430600	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr6:147429400-147430800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr6:147429400-147431600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
50	chr6:147429400-147433000	Enhancers	Primary T cells fromperipheralblood	blood

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