Variant report

Variant	nsv1036843
Chromosome Location	chr12:124122376-124169697
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:506)
CpG islands
(count:795)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:124165973-124166596	GM12878	blood:	n/a	n/a
2	ATF2	chr12:124144752-124145277	GM12878	blood:	n/a	n/a
3	ATF2	chr12:124165813-124166609	GM12878	blood:	n/a	n/a
4	BATF	chr12:124166147-124166490	GM12878	blood:	n/a	n/a
5	BATF	chr12:124166177-124166501	GM12878	blood:	n/a	n/a
6	BATF	chr12:124144904-124145195	GM12878	blood:	n/a	chr12:124145072-124145083
7	BATF	chr12:124144875-124145201	GM12878	blood:	n/a	chr12:124145072-124145083
8	BCL11A	chr12:124166091-124166461	GM12878	blood:	n/a	n/a
9	BCLAF1	chr12:124139925-124140367	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:124166045-124166526	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:124166226-124166361	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:124139600-124140393	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:124146182-124146377	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:124155699-124155729	K562	blood:	n/a	n/a
15	BRCA1	chr12:124133994-124134134	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr12:124147878-124148212	K562	blood:	n/a	n/a
17	CEBPB	chr12:124163883-124164027	K562	blood:	n/a	chr12:124163964-124163975
18	CEBPB	chr12:124155361-124155613	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:124144926-124145288	MCF-7	breast:	n/a	n/a
20	CEBPB	chr12:124144941-124145298	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:124155414-124155714	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:124144822-124145387	A549	lung:	n/a	n/a
23	CEBPB	chr12:124144969-124145294	K562	blood:	n/a	n/a
24	CEBPB	chr12:124146558-124146645	K562	blood:	n/a	chr12:124146632-124146643
25	CEBPB	chr12:124146435-124146820	MCF-7	breast:	n/a	chr12:124146632-124146643
26	CEBPB	chr12:124166291-124166506	HepG2	liver:	n/a	chr12:124166370-124166381
27	CEBPB	chr12:124144925-124145317	IMR90	lung:	n/a	n/a
28	CEBPB	chr12:124155348-124155869	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:124166289-124166474	K562	blood:	n/a	chr12:124166370-124166381
30	CEBPB	chr12:124144946-124145307	A549	lung:	n/a	n/a
31	CEBPB	chr12:124144964-124145165	K562	blood:	n/a	n/a
32	CEBPB	chr12:124146622-124146730	HepG2	liver:	n/a	chr12:124146632-124146643
33	CEBPB	chr12:124166212-124166455	A549	lung:	n/a	chr12:124166370-124166381
34	CEBPB	chr12:124155498-124155638	K562	blood:	n/a	n/a
35	CEBPB	chr12:124163947-124163977	HepG2	liver:	n/a	chr12:124163964-124163975
36	CEBPB	chr12:124166279-124166491	IMR90	lung:	n/a	chr12:124166370-124166381
37	CHD2	chr12:124155480-124155761	K562	blood:	n/a	n/a
38	CHD2	chr12:124140018-124140339	GM12878	blood:	n/a	n/a
39	CHD2	chr12:124155500-124155791	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr12:124155466-124155802	GM12878	blood:	n/a	n/a
41	CHD2	chr12:124155426-124155905	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr12:124155556-124155802	HepG2	liver:	n/a	n/a
43	CREB1	chr12:124155414-124155938	A549	lung:	n/a	n/a
44	CTCF	chr12:124155548-124155706	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr12:124144620-124144770	BJ	skin:	n/a	n/a
46	CTCF	chr12:124133860-124134010	GM12871	blood:	n/a	n/a
47	CTCF	chr12:124151100-124151250	GM12871	blood:	n/a	n/a
48	CTCF	chr12:124141862-124142146	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr12:124151180-124151330	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr12:124151120-124151270	GM12864	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124155712-124155762	HEEpiC	esophagus:	n/a
2	chr12:124145110-124145160	NHDF-neo	bronchial:	n/a
3	chr12:124155712-124155762	HEEpiC	esophagus:	n/a
4	chr12:124145110-124145160	NHDF-neo	bronchial:	n/a
5	chr12:124155594-124155644	BE2_C	brain:	n/a
6	chr12:124155458-124155508	NT2-D1	testis:	n/a
7	chr12:124158499-124158549	GM12878	blood:	n/a
8	chr12:124155579-124155629	HEEpiC	esophagus:	n/a
9	chr12:124155458-124155508	HCPEpiC	choroid plexus:	n/a
10	chr12:124155712-124155762	HMEC	breast:	n/a
11	chr12:124144432-124144482	BJ	skin:	n/a
12	chr12:124155880-124155930	RPTEC	kidney:	n/a
13	chr12:124144432-124144482	SAEC	small airway:	n/a
14	chr12:124155620-124155670	PANC-1	pancreas:	n/a
15	chr12:124144432-124144482	HAEpiC	amniotic membrane:	n/a
16	chr12:124156170-124156220	NT2-D1	testis:	n/a
17	chr12:124158499-124158549	MCF10A-Er-Src	breast:	n/a
18	chr12:124155712-124155762	HL-60	blood:	n/a
19	chr12:124155620-124155670	HCF	heart:	n/a
20	chr12:124145110-124145160	Hepatocyte	liver:	n/a
21	chr12:124156170-124156220	NHDF-neo	bronchial:	n/a
22	chr12:124158499-124158549	HRCEpiC	kidney:	n/a
23	chr12:124155594-124155644	LNCaP	prostate:	n/a
24	chr12:124155458-124155508	A549	lung:	n/a
25	chr12:124158499-124158549	HRE	kidney:	n/a
26	chr12:124156159-124156209	NB4	blood:	n/a
27	chr12:124155880-124155930	SAEC	small airway:	n/a
28	chr12:124144432-124144482	Hepatocyte	liver:	n/a
29	chr12:124155458-124155508	AG09309	skin:	n/a
30	chr12:124156170-124156220	HCT-116	colon:	n/a
31	chr12:124145110-124145160	PANC-1	pancreas:	n/a
32	chr12:124155712-124155762	HCF	heart:	n/a
33	chr12:124158499-124158549	SK-N-MC	brain:	n/a
34	chr12:124155880-124155930	BJ	skin:	n/a
35	chr12:124155594-124155644	HPAEpiC	pulmonary alveolar:	n/a
36	chr12:124155712-124155762	IMR90	lung:	fetal
37	chr12:124156170-124156220	Hepatocyte	liver:	n/a
38	chr12:124155880-124155930	HNPCEpiC	eye:	n/a
39	chr12:124155712-124155762	HUVEC	blood vessel:	n/a
40	chr12:124144432-124144482	SKMC	muscle:	n/a
41	chr12:124156170-124156220	HepG2	liver:	n/a
42	chr12:124144432-124144482	NB4	blood:	n/a
43	chr12:124154378-124154428	BJ	skin:	n/a
44	chr12:124144432-124144482	GM12892	blood:	n/a
45	chr12:124154378-124154428	PFSK-1	brain:	n/a
46	chr12:124156170-124156220	H1-hESC	embryonic stem cell:	embryo
47	chr12:124156159-124156209	ProgFib	skin:	n/a
48	chr12:124144432-124144482	HCF	heart:	n/a
49	chr12:124155594-124155644	HRCEpiC	kidney:	n/a
50	chr12:124144432-124144482	GM12878	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:124117633..124119272-chr12:124133499..124136176,2	K562	blood:
2	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
3	chr12:124117107..124120837-chr12:124123304..124127842,5	MCF-7	breast:
4	chr12:124137919..124140915-chr12:124140949..124142983,2	MCF-7	breast:
5	chr12:124155020..124157089-chr12:124215035..124217819,2	MCF-7	breast:
6	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
7	chr12:124116692..124118630-chr12:124144717..124146823,2	MCF-7	breast:
8	chr12:124154564..124157086-chr12:124160507..124162137,2	MCF-7	breast:
9	chr12:124154247..124158137-chr12:124158575..124163340,6	K562	blood:
10	chr12:124137919..124140915-chr12:124140949..124142983,2	MCF-7	breast:
11	chr12:124130618..124132144-chr12:124154341..124156246,2	MCF-7	breast:
12	chr12:124150219..124152252-chr12:124155815..124157987,2	MCF-7	breast:
13	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
14	chr12:124143980..124146532-chr12:124155769..124157495,2	MCF-7	breast:
15	chr12:124157024..124160371-chr12:124188986..124191737,3	MCF-7	breast:
16	chr12:124150219..124152252-chr12:124155815..124157987,2	MCF-7	breast:
17	chr12:124157626..124159857-chr12:124196461..124198464,2	MCF-7	breast:
18	chr12:124117774..124119426-chr12:124160532..124162075,2	K562	blood:
19	chr12:124134030..124137334-chr12:124197093..124199913,4	MCF-7	breast:
20	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
21	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
22	chr12:124137852..124140530-chr12:124458317..124460698,2	K562	blood:
23	chr12:124157620..124159905-chr12:124196914..124199226,2	K562	blood:
24	chr12:123755242..123756973-chr12:124144725..124146660,2	K562	blood:
25	chr12:124120301..124122353-chr12:124128299..124130201,3	K562	blood:
26	chr12:124117612..124120056-chr12:124127858..124130457,4	K562	blood:
27	chr12:124130507..124132191-chr12:124132895..124134450,2	MCF-7	breast:
28	chr12:124138422..124140008-chr12:124142075..124144430,2	MCF-7	breast:
29	chr12:124131124..124134135-chr12:124154416..124157411,3	K562	blood:
30	chr12:124128608..124131370-chr12:124135245..124137740,4	K562	blood:
31	chr12:124154972..124157295-chr12:124158575..124161176,3	K562	blood:
32	chr12:124157962..124160129-chr12:124161284..124163771,2	MCF-7	breast:
33	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
34	chr12:124095180..124096998-chr12:124140972..124143607,2	MCF-7	breast:
35	chr12:124105734..124108451-chr12:124133249..124135719,2	K562	blood:
36	chr12:124126711..124128243-chr12:124132496..124134774,2	MCF-7	breast:
37	chr12:124116825..124119400-chr12:124154444..124157055,3	MCF-7	breast:
38	chr12:124127308..124129753-chr12:124158031..124160799,2	K562	blood:
39	chr12:124155376..124157580-chr12:124194948..124197481,2	K562	blood:
40	chr12:124084914..124087862-chr12:124122413..124125179,2	K562	blood:
41	chr12:124117712..124121219-chr12:124140785..124143591,3	K562	blood:
42	chr12:124117633..124120865-chr12:124133499..124139438,5	K562	blood:
43	chr12:124154048..124155942-chr12:124162322..124165220,2	K562	blood:
44	chr12:124118193..124121025-chr12:124132767..124136539,4	MCF-7	breast:
45	chr12:124150313..124152080-chr12:124154611..124157419,2	MCF-7	breast:
46	chr12:124117920..124120001-chr12:124129132..124130798,2	MCF-7	breast:
47	chr12:124125615..124128872-chr12:124133075..124135751,3	MCF-7	breast:
48	chr12:124155686..124156232-chr17:56084289..56085093,2	HCT-116	colon:
49	chr12:124123949..124126710-chr12:124128875..124131426,2	K562	blood:
50	chr12:124155436..124158746-chr12:124195101..124198299,4	MCF-7	breast:

No data

Variant related genes	Relation type
EIF2B1	TF binding region
GTF2H3	TF binding region
TCTN2	TF binding region
EIF2B1	CpG island
GTF2H3	CpG island
TCTN2	CpG island
ENSG00000111328	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000111358	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000168778	chromatin interactions
ENSG00000185344	chromatin interactions

Extended variants
information (count: 1865 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1865 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536480775	chr12:124122386-124122387	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs555073072	chr12:124122405-124122406	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs11057312	chr12:124122408-124122409	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs189133924	chr12:124122422-124122423	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs202238371	chr12:124122531-124122532	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs529751748	chr12:124122534-124122535	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs374610567	chr12:124122550-124122551	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs541936638	chr12:124122606-124122607	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs181833286	chr12:124122619-124122620	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs545268611	chr12:124122648-124122649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11572928	chr12:124122663-124122664	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs575364928	chr12:124122664-124122665	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542432609	chr12:124122674-124122675	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145545471	chr12:124122683-124122684	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376668603	chr12:124122695-124122696	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs562186268	chr12:124122746-124122747	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs527801944	chr12:124122777-124122778	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs539978260	chr12:124122792-124122793	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs558778665	chr12:124122793-124122794	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs575721533	chr12:124122798-124122799	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs564893130	chr12:124122815-124122816	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs537834603	chr12:124122858-124122859	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs369949498	chr12:124122918-124122919	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs11572929	chr12:124122937-124122938	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs569472661	chr12:124122948-124122949	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs138152147	chr12:124122987-124122988	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs138864802	chr12:124122997-124122998	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs377651178	chr12:124123007-124123008	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs7306528	chr12:124123008-124123009	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs534287537	chr12:124123009-124123010	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs558815005	chr12:124123013-124123014	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs570812044	chr12:124123014-124123015	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs11572931	chr12:124123070-124123071	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs370929671	chr12:124123088-124123089	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs78393433	chr12:124123135-124123136	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs575450291	chr12:124123150-124123151	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs146050590	chr12:124123163-124123164	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs554333022	chr12:124123266-124123267	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs187388252	chr12:124123273-124123274	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs377373697	chr12:124123285-124123286	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148720312	chr12:124123302-124123303	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546734869	chr12:124123311-124123312	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs79497521	chr12:124123339-124123340	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374933799	chr12:124123340-124123341	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs75691495	chr12:124123342-124123343	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs543701331	chr12:124123404-124123405	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs141444558	chr12:124123412-124123413	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs112183155	chr12:124123436-124123437	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs548947813	chr12:124123444-124123445	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs111494960	chr12:124123456-124123457	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1889 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124119200-124124400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:124119200-124129800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:124119200-124129800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:124119200-124130000	Weak transcription	Pancreas	Pancrea
5	chr12:124119200-124130200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:124119200-124130200	Weak transcription	Right Ventricle	heart
7	chr12:124119200-124141000	Weak transcription	Aorta	Aorta
8	chr12:124119200-124155200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr12:124119400-124123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:124119400-124123800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr12:124119400-124124000	Weak transcription	Esophagus	oesophagus
12	chr12:124119400-124124400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:124119400-124124400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr12:124119400-124124600	Weak transcription	Fetal Intestine Large	intestine
15	chr12:124119400-124124600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr12:124119400-124127200	Weak transcription	Placenta	Placenta
17	chr12:124119400-124129600	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr12:124119400-124129600	Weak transcription	HSMMtube	muscle
19	chr12:124119400-124129800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:124119400-124129800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr12:124119400-124129800	Weak transcription	Lung	lung
22	chr12:124119400-124129800	Weak transcription	Ovary	ovary
23	chr12:124119400-124130200	Weak transcription	Fetal Kidney	kidney
24	chr12:124119400-124130200	Weak transcription	Gastric	stomach
25	chr12:124119400-124131200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:124119400-124132000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr12:124119600-124123000	Weak transcription	Fetal Intestine Small	intestine
28	chr12:124119600-124123200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:124119600-124123600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr12:124119600-124123800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr12:124119600-124124000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr12:124119600-124124000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr12:124119600-124124000	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr12:124119600-124124000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr12:124119600-124124000	Weak transcription	Fetal Thymus	thymus
36	chr12:124119600-124124200	Weak transcription	Primary B cells from peripheral blood	blood
37	chr12:124119600-124124200	Weak transcription	Fetal Brain Male	brain
38	chr12:124119600-124124400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:124119600-124124400	Weak transcription	Brain Substantia Nigra	brain
40	chr12:124119600-124124400	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr12:124119600-124124400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr12:124119600-124124400	Weak transcription	Thymus	Thymus
43	chr12:124119600-124124600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr12:124119600-124125200	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr12:124119600-124126200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr12:124119600-124126600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr12:124119600-124126600	Weak transcription	Primary hematopoietic stem cells	blood
48	chr12:124119600-124126600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr12:124119600-124126800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr12:124119600-124126800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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