Variant report

Variant	esv1001176
Chromosome Location	chr4:124977327-124988425
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:124981440-124981590	AG10803	skin:	n/a	n/a
2	CTCF	chr4:124981680-124981830	HPAF	blood vessel:	n/a	n/a
3	EP300	chr4:124981503-124981886	SK-N-SH_RA	brain:	n/a	chr4:124981834-124981848 chr4:124981852-124981862 chr4:124981511-124981525
4	EP300	chr4:124981408-124982086	SK-N-SH_RA	brain:	n/a	chr4:124981834-124981848 chr4:124981852-124981862 chr4:124981956-124981966 chr4:124981511-124981525
5	EP300	chr4:124981341-124982394	SK-N-SH	brain:	n/a	chr4:124981834-124981848 chr4:124982380-124982394 chr4:124981852-124981862 chr4:124981956-124981966 chr4:124981511-124981525
6	EP300	chr4:124982241-124982269	K562	blood:	n/a	n/a
7	FOS	chr4:124981344-124981814	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr4:124981344-124981656	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr4:124981299-124981631	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr4:124981310-124981861	HUVEC	blood vessel:	n/a	n/a
11	FOS	chr4:124981343-124981674	MCF10A-Er-Src	breast:	n/a	n/a
12	GATA1	chr4:124981359-124981942	PBDE	blood:	n/a	chr4:124981587-124981594
13	GATA3	chr4:124981317-124982473	SK-N-SH	brain:	n/a	chr4:124982113-124982120 chr4:124981587-124981594
14	GATA3	chr4:124981329-124982466	SK-N-SH	brain:	n/a	chr4:124982113-124982120 chr4:124981587-124981594
15	GATA3	chr4:124981445-124981769	SH-SY5Y	brain:	n/a	chr4:124981587-124981594
16	GATA3	chr4:124982003-124982203	SH-SY5Y	brain:	n/a	chr4:124982113-124982120
17	MYC	chr4:124981920-124982112	MCF10A-Er-Src	breast:	n/a	n/a
18	PBX3	chr4:124981495-124982314	SK-N-SH	brain:	n/a	n/a
19	POLR2A	chr4:124981388-124981693	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr4:124980240-124980319	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr4:124981602-124981749	SK-N-SH	brain:	n/a	n/a
22	POLR2A	chr4:124981593-124981677	ProgFib	skin:	n/a	n/a
23	POLR2A	chr4:124981718-124981842	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr4:124982106-124982135	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr4:124981426-124981994	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr4:124981312-124981895	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr4:124982529-124982953	SK-N-MC	brain:	n/a	n/a
28	POLR2A	chr4:124982499-124983009	MCF10A-Er-Src	breast:	n/a	n/a
29	RAD21	chr4:124981555-124981882	SK-N-SH_RA	brain:	n/a	n/a
30	RAD21	chr4:124981552-124981901	SK-N-SH_RA	brain:	n/a	n/a
31	SPI1	chr4:124987108-124987370	GM12878	blood:	n/a	n/a
32	SPI1	chr4:124981671-124981892	GM12891	blood:	n/a	n/a
33	SPI1	chr4:124981563-124982302	HL-60	blood:	n/a	chr4:124982040-124982053
34	SPI1	chr4:124981647-124981903	GM12878	blood:	n/a	n/a
35	SPI1	chr4:124987130-124987295	K562	blood:	n/a	n/a
36	SPI1	chr4:124987138-124987319	K562	blood:	n/a	n/a
37	SPI1	chr4:124981602-124982250	HL-60	blood:	n/a	chr4:124982040-124982053
38	STAT3	chr4:124981338-124981541	MCF10A-Er-Src	breast:	n/a	n/a
39	STAT3	chr4:124981442-124981642	MCF10A-Er-Src	breast:	n/a	n/a
40	STAT3	chr4:124981406-124981543	MCF10A-Er-Src	breast:	n/a	n/a
41	TAF1	chr4:124981628-124981829	SK-N-SH	brain:	n/a	n/a
42	TCF12	chr4:124981313-124982462	SK-N-SH	brain:	n/a	n/a
43	TCF12	chr4:124981461-124982270	SK-N-SH	brain:	n/a	n/a
44	TCF7L2	chr4:124981781-124982161	PANC-1	pancreas:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:124983615-124983665	HepG2	liver:	n/a
2	chr4:124983615-124983665	SAEC	small airway:	n/a
3	chr4:124983615-124983665	GM12892	blood:	n/a
4	chr4:124983615-124983665	H1-hESC	embryonic stem cell:	embryo
5	chr4:124983615-124983665	SK-N-SH_RA	brain:	n/a
6	chr4:124983615-124983665	GM19239	blood:	n/a
7	chr4:124983615-124983665	A549	lung:	n/a
8	chr4:124983615-124983665	GM12878	blood:	n/a
9	chr4:124983615-124983665	AG04449	skin:	fetal
10	chr4:124983615-124983665	NH-A	brain:	n/a
11	chr4:124983615-124983665	ECC-1	luminal epithelium:	n/a
12	chr4:124983615-124983665	BE2_C	brain:	n/a
13	chr4:124983615-124983665	HUVEC	blood vessel:	n/a
14	chr4:124983615-124983665	HCM	heart:	n/a
15	chr4:124983615-124983665	IMR90	lung:	fetal
16	chr4:124983615-124983665	NHBE	bronchial:	n/a
17	chr4:124983615-124983665	HL-60	blood:	n/a
18	chr4:124983615-124983665	HIPEpiC	eye:	n/a
19	chr4:124983615-124983665	HCPEpiC	choroid plexus:	n/a
20	chr4:124983615-124983665	ovcar-3	ovarian:	n/a
21	chr4:124983615-124983665	NT2-D1	testis:	n/a
22	chr4:124983615-124983665	GM06990	blood:	n/a
23	chr4:124983615-124983665	HNPCEpiC	eye:	n/a
24	chr4:124983615-124983665	U87	brain:	n/a
25	chr4:124983615-124983665	MCF10A-Er-Src	breast:	n/a
26	chr4:124983615-124983665	HCT-116	colon:	n/a
27	chr4:124983615-124983665	K562	blood:	n/a
28	chr4:124983615-124983665	HPAEpiC	pulmonary alveolar:	n/a
29	chr4:124983615-124983665	BJ	skin:	n/a
30	chr4:124983615-124983665	PFSK-1	brain:	n/a
31	chr4:124983615-124983665	HAEpiC	amniotic membrane:	n/a
32	chr4:124983615-124983665	SKMC	muscle:	n/a
33	chr4:124983615-124983665	PANC-1	pancreas:	n/a
34	chr4:124983615-124983665	HMEC	breast:	n/a
35	chr4:124983615-124983665	HEK293	kidney:	embryo
36	chr4:124983615-124983665	SK-N-MC	brain:	n/a
37	chr4:124983615-124983665	Jurkat	blood:	n/a
38	chr4:124983615-124983665	PrEC	prostate:	n/a
39	chr4:124983615-124983665	AG10803	skin:	n/a
40	chr4:124983615-124983665	HCF	heart:	n/a
41	chr4:124983615-124983665	HRE	kidney:	n/a
42	chr4:124983615-124983665	ProgFib	skin:	n/a
43	chr4:124983615-124983665	LNCaP	prostate:	n/a
44	chr4:124983615-124983665	NB4	blood:	n/a
45	chr4:124983615-124983665	Hela-S3	cervix:	n/a
46	chr4:124983615-124983665	RPTEC	kidney:	n/a
47	chr4:124983615-124983665	SK-N-SH	brain:	n/a
48	chr4:124983615-124983665	AG09309	skin:	n/a
49	chr4:124983615-124983665	CMK	blood:	n/a
50	chr4:124983615-124983665	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:124981418..124984349-chr4:124987822..124990040,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPRY1-8	chr4:124983617-124984145	NONHSAT098211

No data

Variant related genes	Relation type
ENSG00000250484	TF binding region
ENSG00000250484	CpG island
ENSG00000250484	chromatin interactions

Extended variants
information (count: 389 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551836830	chr4:124977348-124977349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs62319999	chr4:124977422-124977423	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534141285	chr4:124977447-124977448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553783420	chr4:124977495-124977496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188161565	chr4:124977504-124977505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150207687	chr4:124977559-124977560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139166590	chr4:124977619-124977620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1028197	chr4:124977659-124977660	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs190852551	chr4:124977670-124977671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113290492	chr4:124977672-124977673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140362211	chr4:124977675-124977676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs1028198	chr4:124977734-124977735	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs74808810	chr4:124977746-124977747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560637631	chr4:124977749-124977750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529563471	chr4:124977766-124977767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142963206	chr4:124977771-124977772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373464296	chr4:124977803-124977804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542883745	chr4:124977805-124977806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147466315	chr4:124977856-124977857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1028199	chr4:124977880-124977881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551903125	chr4:124977891-124977892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73846837	chr4:124977932-124977933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369261278	chr4:124977934-124977935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187908815	chr4:124977965-124977966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192692475	chr4:124978002-124978003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527693573	chr4:124978022-124978023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs17813733	chr4:124978059-124978060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560735843	chr4:124978064-124978065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114575629	chr4:124978081-124978082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536524602	chr4:124978088-124978089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555973320	chr4:124978095-124978096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140588230	chr4:124978098-124978099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117191400	chr4:124978142-124978143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574331417	chr4:124978147-124978148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184883910	chr4:124978267-124978268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187625029	chr4:124978276-124978277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77096433	chr4:124978298-124978299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79423468	chr4:124978353-124978354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574289189	chr4:124978416-124978417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs377351554	chr4:124978444-124978445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543336884	chr4:124978454-124978455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117534446	chr4:124978466-124978467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144618603	chr4:124978542-124978543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532841637	chr4:124978591-124978592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs193063385	chr4:124978613-124978614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1401535	chr4:124978662-124978663	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs148442806	chr4:124978749-124978750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114911356	chr4:124978767-124978768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184854940	chr4:124978819-124978820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529983270	chr4:124978845-124978846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124975200-124981600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:124975600-124977600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:124975600-124981000	Weak transcription	HUVEC	blood vessel
4	chr4:124976000-124977800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr4:124976400-124977400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:124976400-124977400	Enhancers	Osteobl	bone
7	chr4:124976400-124977800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:124976600-124977400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:124976600-124977400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:124976800-124977400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:124976800-124981400	Weak transcription	NHDF-Ad	bronchial
12	chr4:124976800-124981400	Weak transcription	NHLF	lung
13	chr4:124976800-124981600	Weak transcription	Aorta	Aorta
14	chr4:124977400-124979800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:124977400-124981000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:124977400-124981600	Weak transcription	Osteobl	bone
17	chr4:124977600-124981400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr4:124977800-124980600	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr4:124977800-124981400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr4:124978400-124979200	Enhancers	Colon Smooth Muscle	Colon
21	chr4:124979200-124981400	Weak transcription	Colon Smooth Muscle	Colon
22	chr4:124979800-124980200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:124980000-124980200	ZNF genes & repeats	Fetal Lung	lung
24	chr4:124980200-124980800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr4:124980200-124981400	Weak transcription	Fetal Lung	lung
26	chr4:124980400-124981400	Weak transcription	Adipose Nuclei	Adipose
27	chr4:124980400-124981400	Weak transcription	Fetal Heart	heart
28	chr4:124980600-124981600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr4:124980800-124981800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:124981000-124981400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr4:124981000-124981600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:124981000-124981600	Enhancers	HUVEC	blood vessel
33	chr4:124981000-124982400	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr4:124981000-124982800	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr4:124981000-124983000	Enhancers	HSMMtube	muscle
36	chr4:124981000-124983400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr4:124981000-124984200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:124981200-124982200	Enhancers	Primary hematopoietic stem cells	blood
39	chr4:124981400-124981600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:124981400-124981600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:124981400-124981600	Enhancers	Adipose Nuclei	Adipose
42	chr4:124981400-124981600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr4:124981400-124981600	Enhancers	NHEK	skin
44	chr4:124981400-124981600	Enhancers	NHLF	lung
45	chr4:124981400-124981800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr4:124981400-124981800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr4:124981400-124982000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:124981400-124982200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr4:124981400-124982400	Enhancers	Colon Smooth Muscle	Colon
50	chr4:124981400-124982400	Enhancers	Fetal Heart	heart

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