Variant report

Variant	esv3354568
Chromosome Location	chr1:9593665-9598963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:9596417-9596453	K562	blood:	n/a	n/a
2	ARID3A	chr1:9597804-9598357	HepG2	liver:	n/a	n/a
3	BHLHE40	chr1:9598963-9600458	K562	blood:	n/a	chr1:9599494-9599507
4	CBX3	chr1:9598786-9599532	K562	blood:	n/a	n/a
5	CCNT2	chr1:9598904-9600430	K562	blood:	n/a	chr1:9600151-9600160 chr1:9600145-9600154
6	CEBPB	chr1:9597942-9598250	HepG2	liver:	n/a	chr1:9598084-9598096
7	CEBPB	chr1:9596259-9596434	K562	blood:	n/a	n/a
8	CEBPD	chr1:9598043-9598407	HepG2	liver:	n/a	n/a
9	CEBPD	chr1:9598849-9599624	K562	blood:	n/a	n/a
10	CEBPD	chr1:9597917-9598226	HepG2	liver:	n/a	n/a
11	CHD2	chr1:9598932-9599612	GM12878	blood:	n/a	chr1:9599449-9599459
12	CHD2	chr1:9598186-9599600	K562	blood:	n/a	chr1:9599449-9599459
13	CHD2	chr1:9598092-9598431	HepG2	liver:	n/a	n/a
14	CREB1	chr1:9598851-9600457	HepG2	liver:	n/a	chr1:9599472-9599485
15	CREB1	chr1:9598961-9599746	HepG2	liver:	n/a	chr1:9599472-9599485
16	CTCF	chr1:9598560-9598710	WERI-Rb-1	eye:	n/a	n/a
17	CTCF	chr1:9598471-9598498	Spleen_OC	spleen:	n/a	n/a
18	CUX1	chr1:9596322-9596380	K562	blood:	n/a	n/a
19	E2F6	chr1:9598946-9599694	A549	lung:	n/a	chr1:9599473-9599482 chr1:9599475-9599484
20	E2F6	chr1:9598943-9599723	H1-hESC	embryonic stem cell:	n/a	chr1:9599473-9599482 chr1:9599475-9599484
21	E2F6	chr1:9598920-9599115	K562	blood:	n/a	n/a
22	E2F6	chr1:9598909-9600485	K562	blood:	n/a	chr1:9600151-9600160 chr1:9599918-9599927 chr1:9600034-9600043 chr1:9599739-9599748 chr1:9599473-9599482 chr1:9600148-9600160 chr1:9599475-9599484
23	E2F6	chr1:9598908-9599594	H1-hESC	embryonic stem cell:	n/a	chr1:9599473-9599482 chr1:9599475-9599484
24	ELF1	chr1:9597940-9598454	HepG2	liver:	n/a	n/a
25	ELF1	chr1:9598083-9598453	K562	blood:	n/a	n/a
26	ELF1	chr1:9597938-9598437	HepG2	liver:	n/a	n/a
27	EP300	chr1:9598914-9599605	K562	blood:	n/a	chr1:9599488-9599497
28	EP300	chr1:9597823-9598489	HepG2	liver:	n/a	chr1:9598183-9598197
29	EP300	chr1:9597931-9598404	HepG2	liver:	n/a	chr1:9598183-9598197
30	EP300	chr1:9597873-9598387	HepG2	liver:	n/a	chr1:9598183-9598197
31	FOXA1	chr1:9597762-9598423	HepG2	liver:	n/a	chr1:9598116-9598131
32	FOXA1	chr1:9597983-9598392	T-47D	breast:	n/a	chr1:9598116-9598131
33	FOXA1	chr1:9597995-9598316	T-47D	breast:	n/a	chr1:9598116-9598131
34	FOXA1	chr1:9597831-9598445	HepG2	liver:	n/a	chr1:9598116-9598131
35	FOXA1	chr1:9598904-9599349	HepG2	liver:	n/a	n/a
36	FOXA1	chr1:9597765-9598524	HepG2	liver:	n/a	chr1:9598116-9598131
37	FOXA1	chr1:9597767-9598630	HepG2	liver:	n/a	chr1:9598116-9598131
38	FOXA1	chr1:9598815-9599685	HepG2	liver:	n/a	n/a
39	FOXA2	chr1:9597812-9598394	HepG2	liver:	n/a	n/a
40	FOXA2	chr1:9597626-9598729	HepG2	liver:	n/a	n/a
41	GATA1	chr1:9598740-9600319	PBDE	blood:	n/a	n/a
42	GATA3	chr1:9598168-9598475	T-47D	breast:	n/a	n/a
43	HCFC1	chr1:9598952-9599904	Hela-S3	cervix:	n/a	n/a
44	HDAC2	chr1:9597873-9598473	HepG2	liver:	n/a	chr1:9597906-9597920 chr1:9597910-9597924
45	HDAC2	chr1:9597856-9598428	HepG2	liver:	n/a	chr1:9597906-9597920 chr1:9597910-9597924
46	HEY1	chr1:9598094-9598427	K562	blood:	n/a	n/a
47	HEY1	chr1:9598812-9600545	K562	blood:	n/a	chr1:9599507-9599522 chr1:9599473-9599482 chr1:9599541-9599556 chr1:9599505-9599520 chr1:9599532-9599547 chr1:9599909-9599924 chr1:9599475-9599484
48	HEY1	chr1:9598843-9600412	K562	blood:	n/a	chr1:9599507-9599522 chr1:9599473-9599482 chr1:9599541-9599556 chr1:9599505-9599520 chr1:9599532-9599547 chr1:9599909-9599924 chr1:9599475-9599484
49	HEY1	chr1:9598751-9599831	HepG2	liver:	n/a	chr1:9599507-9599522 chr1:9599473-9599482 chr1:9599541-9599556 chr1:9599505-9599520 chr1:9599532-9599547 chr1:9599475-9599484
50	HEY1	chr1:9597776-9598737	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:9598932-9598982	AoSMC	blood vessel:	n/a
2	chr1:9598932-9598982	AoSMC	blood vessel:	n/a
3	chr1:9598932-9598982	SKMC	muscle:	n/a
4	chr1:9598932-9598982	Hepatocyte	liver:	n/a
5	chr1:9598932-9598982	HCF	heart:	n/a
6	chr1:9598932-9598982	Caco-2	colon:	n/a
7	chr1:9598932-9598982	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:9598932-9598982	MCF10A-Er-Src	breast:	n/a
9	chr1:9598932-9598982	A549	lung:	n/a
10	chr1:9598932-9598982	HEEpiC	esophagus:	n/a
11	chr1:9598932-9598982	NB4	blood:	n/a
12	chr1:9598932-9598982	SK-N-SH_RA	brain:	n/a
13	chr1:9598932-9598982	RPTEC	kidney:	n/a
14	chr1:9598932-9598982	BE2_C	brain:	n/a
15	chr1:9598932-9598982	ProgFib	skin:	n/a
16	chr1:9598932-9598982	HUVEC	blood vessel:	n/a
17	chr1:9598932-9598982	U87	brain:	n/a
18	chr1:9598932-9598982	GM12891	blood:	n/a
19	chr1:9598932-9598982	PANC-1	pancreas:	n/a
20	chr1:9598932-9598982	HRCEpiC	kidney:	n/a
21	chr1:9598932-9598982	IMR90	lung:	fetal
22	chr1:9598932-9598982	T-47D	breast:	n/a
23	chr1:9598932-9598982	NH-A	brain:	n/a
24	chr1:9598932-9598982	HCT-116	colon:	n/a
25	chr1:9598932-9598982	AG09319	gingival:	n/a
26	chr1:9598932-9598982	HIPEpiC	eye:	n/a
27	chr1:9598932-9598982	NHDF-neo	bronchial:	n/a
28	chr1:9598932-9598982	Hela-S3	cervix:	n/a
29	chr1:9598932-9598982	SAEC	small airway:	n/a
30	chr1:9598932-9598982	HMEC	breast:	n/a
31	chr1:9598932-9598982	HRE	kidney:	n/a
32	chr1:9598932-9598982	ovcar-3	ovarian:	n/a
33	chr1:9598932-9598982	BJ	skin:	n/a
34	chr1:9598932-9598982	PFSK-1	brain:	n/a
35	chr1:9598932-9598982	AG04450	lung:	fetal
36	chr1:9598932-9598982	GM12878	blood:	n/a
37	chr1:9598932-9598982	HAEpiC	amniotic membrane:	n/a
38	chr1:9598932-9598982	PrEC	prostate:	n/a
39	chr1:9598932-9598982	GM12892	blood:	n/a
40	chr1:9598932-9598982	CMK	blood:	n/a
41	chr1:9598932-9598982	HEK293	kidney:	embryo
42	chr1:9598932-9598982	MCF-7	breast:	n/a
43	chr1:9598932-9598982	SK-N-SH	brain:	n/a
44	chr1:9598932-9598982	AG04449	skin:	fetal
45	chr1:9598932-9598982	GM06990	blood:	n/a
46	chr1:9598932-9598982	HNPCEpiC	eye:	n/a
47	chr1:9598932-9598982	HL-60	blood:	n/a
48	chr1:9598932-9598982	HCM	heart:	n/a
49	chr1:9598932-9598982	HRPEpiC	eye:	n/a
50	chr1:9598932-9598982	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:9593476..9595125-chr1:9597085..9600029,2	K562	blood:
2	chr1:9350586..9353918-chr1:9597167..9600975,3	MCF-7	breast:
3	chr1:9340527..9342561-chr1:9591961..9594805,2	K562	blood:
4	chr1:9597781..9602686-chr1:9646599..9652829,9	K562	blood:
5	chr1:9588957..9591794-chr1:9592247..9595158,3	K562	blood:
6	chr1:9597937..9599836-chr1:9648693..9652829,4	K562	blood:
7	chr1:9594978..9597511-chr1:9598166..9600611,4	K562	blood:
8	chr1:9588042..9590457-chr1:9592247..9594686,2	K562	blood:
9	chr1:9589698..9594736-chr1:9596455..9600782,9	K562	blood:
10	chr1:9597734..9599433-chr1:9617661..9619736,2	K562	blood:
11	chr1:9596866..9598419-chr1:9883166..9885475,2	K562	blood:
12	chr1:9294638..9296253-chr1:9598479..9600330,2	K562	blood:
13	chr1:9586876..9589181-chr1:9596662..9599409,2	K562	blood:
14	chr1:9594867..9596553-chr1:9616924..9619437,2	MCF-7	breast:

Variant related genes	Relation type
SLC25A33	TF binding region
SLC25A33	CpG island
ENSG00000171603	chromatin interactions
ENSG00000188807	chromatin interactions
ENSG00000049239	chromatin interactions
ENSG00000171621	chromatin interactions
ENSG00000171612	chromatin interactions

Extended variants
information (count: 172 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:172 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569125387	chr1:9593692-9593693	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs55780537	chr1:9593702-9593703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558876031	chr1:9593717-9593718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs55986711	chr1:9593797-9593798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs541494738	chr1:9593882-9593883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566519152	chr1:9593952-9593953	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534758245	chr1:9593995-9593996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371294800	chr1:9594005-9594006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs373334785	chr1:9594051-9594052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574682969	chr1:9594061-9594062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552928853	chr1:9594094-9594095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563644369	chr1:9594107-9594108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531210814	chr1:9594111-9594112	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545499908	chr1:9594112-9594113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs564085836	chr1:9594140-9594141	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs184493263	chr1:9594183-9594184	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144657787	chr1:9594195-9594196	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568121533	chr1:9594228-9594229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs12136603	chr1:9594278-9594279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12136605	chr1:9594309-9594310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113476517	chr1:9594358-9594359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs550766412	chr1:9594402-9594403	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs141257410	chr1:9594418-9594419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539706198	chr1:9594461-9594462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs77048253	chr1:9594472-9594473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150759642	chr1:9594473-9594474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75315738	chr1:9594475-9594476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs79840762	chr1:9594483-9594484	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs80198604	chr1:9594485-9594486	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs61394664	chr1:9594534-9594535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188858940	chr1:9594536-9594537	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534847176	chr1:9594537-9594538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374685621	chr1:9594544-9594545	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs181200071	chr1:9594545-9594546	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574547933	chr1:9594559-9594560	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs58416959	chr1:9594590-9594591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535676564	chr1:9594601-9594602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557101247	chr1:9594631-9594632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138093723	chr1:9594659-9594660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs577537148	chr1:9594660-9594661	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12037667	chr1:9594670-9594671	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs553788378	chr1:9594671-9594672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572804138	chr1:9594766-9594767	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540188615	chr1:9594787-9594788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561788548	chr1:9594788-9594789	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376930168	chr1:9594792-9594793	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs550827419	chr1:9594842-9594843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562681977	chr1:9594890-9594891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186209770	chr1:9594896-9594897	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369417118	chr1:9594904-9594905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9555800-9599400	Weak transcription	Right Atrium	heart
2	chr1:9587200-9598200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:9591600-9598200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:9591600-9599000	Weak transcription	Adipose Nuclei	Adipose
5	chr1:9591600-9599400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr1:9592000-9598000	Weak transcription	Fetal Heart	heart
7	chr1:9592600-9594400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:9592800-9594600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:9593000-9593800	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr1:9593200-9598600	Weak transcription	Brain Anterior Caudate	brain
11	chr1:9593200-9599000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr1:9593400-9593800	Enhancers	HepG2	liver
13	chr1:9593400-9597800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr1:9593400-9597800	Weak transcription	Liver	Liver
15	chr1:9593400-9598000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr1:9593400-9598400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr1:9593400-9598600	Weak transcription	Fetal Lung	lung
18	chr1:9593400-9598800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:9593400-9598800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr1:9593400-9598800	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr1:9593600-9596200	Weak transcription	Fetal Intestine Small	intestine
22	chr1:9593600-9597200	Weak transcription	Fetal Intestine Large	intestine
23	chr1:9593600-9598000	Weak transcription	Brain Substantia Nigra	brain
24	chr1:9593600-9598200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr1:9593600-9598200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:9593600-9598400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr1:9593600-9598800	Weak transcription	Brain Hippocampus Middle	brain
28	chr1:9593600-9599000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:9593600-9599000	Weak transcription	Brain Angular Gyrus	brain
30	chr1:9593600-9599600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:9593800-9596400	Weak transcription	HepG2	liver
32	chr1:9593800-9599000	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr1:9594400-9599400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr1:9594600-9599000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:9595800-9596000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:9596200-9596400	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr1:9596200-9597000	Enhancers	Fetal Intestine Small	intestine
38	chr1:9596200-9599400	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr1:9596400-9597800	Enhancers	HepG2	liver
40	chr1:9596800-9598000	Weak transcription	Pancreatic Islets	Pancreatic Islet
41	chr1:9597000-9597800	Weak transcription	Fetal Intestine Small	intestine
42	chr1:9597200-9597800	Enhancers	Fetal Intestine Large	intestine
43	chr1:9597200-9599200	Enhancers	Stomach Mucosa	stomach
44	chr1:9597600-9597800	Enhancers	Duodenum Mucosa	Duodenum
45	chr1:9597800-9598000	Flanking Active TSS	Liver	Liver
46	chr1:9597800-9598000	Enhancers	Fetal Intestine Small	intestine
47	chr1:9597800-9598000	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr1:9597800-9598200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr1:9597800-9598200	Enhancers	Small Intestine	intestine
50	chr1:9597800-9598400	Flanking Active TSS	Duodenum Mucosa	Duodenum

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