Variant report

Variant	nsv1007665
Chromosome Location	chr3:21781727-21809266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:612)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:21792431-21793017	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr3:21782837-21782869	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr3:21792339-21792940	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr3:21792482-21792673	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr3:21792005-21792065	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr3:21792301-21793038	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr3:21792360-21793085	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr3:21792463-21792984	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr3:21792388-21792991	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr3:21794340-21794490	NHLF	lung:	n/a	n/a
11	CTCF	chr3:21794380-21794530	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr3:21794351-21794539	HepG2	liver:	n/a	n/a
13	CTCF	chr3:21794360-21794510	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr3:21794521-21794522	GM10248	blood:	n/a	n/a
15	CTCF	chr3:21792633-21792690	Fibrobl	skin:	n/a	n/a
16	CTCF	chr3:21794320-21794470	NHEK	skin:	n/a	n/a
17	CTCF	chr3:21794360-21794510	HCM	heart:	n/a	n/a
18	CTCF	chr3:21794302-21794577	LNCaP	prostate:	n/a	n/a
19	CTCF	chr3:21794309-21794580	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr3:21794360-21794510	GM12874	blood:	n/a	n/a
21	CTCF	chr3:21794360-21794510	GM12868	blood:	n/a	n/a
22	CTCF	chr3:21794360-21794510	GM12875	blood:	n/a	n/a
23	CTCF	chr3:21794380-21794530	HAc	cerebellar:	n/a	n/a
24	CTCF	chr3:21792500-21792650	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr3:21794440-21794590	HCT-116	colon:	n/a	n/a
26	CTCF	chr3:21794360-21794510	AG04450	lung:	n/a	n/a
27	CTCF	chr3:21794420-21794570	BJ	skin:	n/a	n/a
28	CTCF	chr3:21794400-21794550	AG09309	skin:	n/a	n/a
29	CTCF	chr3:21794347-21794548	ECC-1	luminal epithelium:	n/a	n/a
30	CTCF	chr3:21794360-21794510	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr3:21792460-21792610	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr3:21794360-21794510	Caco-2	colon:	n/a	n/a
33	CTCF	chr3:21794340-21794490	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr3:21794240-21794390	HCT-116	colon:	n/a	n/a
35	CTCF	chr3:21794360-21794510	HMEC	breast:	n/a	n/a
36	CTCF	chr3:21794360-21794510	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr3:21794380-21794530	GM12864	blood:	n/a	n/a
38	CTCF	chr3:21794363-21794512	GM19239	blood:	n/a	n/a
39	CTCF	chr3:21794331-21794540	GM10266	blood:	n/a	n/a
40	CTCF	chr3:21794316-21794572	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr3:21794360-21794510	K562	blood:	n/a	n/a
42	CTCF	chr3:21794360-21794510	HPF	lung:	n/a	n/a
43	CTCF	chr3:21794360-21794510	SAEC	small airway:	n/a	n/a
44	CTCF	chr3:21794328-21794538	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr3:21794440-21794590	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr3:21794380-21794530	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr3:21794400-21794550	HL-60	blood:	n/a	n/a
48	CTCF	chr3:21794232-21794590	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:21794380-21794530	BJ	skin:	n/a	n/a
50	CTCF	chr3:21793366-21794946	SK-N-SH	brain:	n/a	chr3:21794209-21794218

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21792248-21792298	HMEC	breast:	n/a
2	chr3:21792991-21793041	NHDF-neo	bronchial:	n/a
3	chr3:21792248-21792298	HMEC	breast:	n/a
4	chr3:21792991-21793041	NHDF-neo	bronchial:	n/a
5	chr3:21792684-21792734	SK-N-SH	brain:	n/a
6	chr3:21792857-21792907	HCM	heart:	n/a
7	chr3:21792684-21792734	HIPEpiC	eye:	n/a
8	chr3:21792857-21792907	GM12878	blood:	n/a
9	chr3:21793557-21793607	GM06990	blood:	n/a
10	chr3:21792938-21792988	MCF-7	breast:	n/a
11	chr3:21792991-21793041	HL-60	blood:	n/a
12	chr3:21792434-21792484	K562	blood:	n/a
13	chr3:21792965-21793015	BJ	skin:	n/a
14	chr3:21792991-21793041	ovcar-3	ovarian:	n/a
15	chr3:21792965-21793015	U87	brain:	n/a
16	chr3:21792857-21792907	K562	blood:	n/a
17	chr3:21792991-21793041	HCM	heart:	n/a
18	chr3:21792248-21792298	ECC-1	luminal epithelium:	n/a
19	chr3:21790232-21790282	HIPEpiC	eye:	n/a
20	chr3:21792857-21792907	SKMC	muscle:	n/a
21	chr3:21792434-21792484	AG09319	gingival:	n/a
22	chr3:21793557-21793607	HL-60	blood:	n/a
23	chr3:21792991-21793041	HRCEpiC	kidney:	n/a
24	chr3:21792434-21792484	Hepatocyte	liver:	n/a
25	chr3:21792857-21792907	CMK	blood:	n/a
26	chr3:21793557-21793607	A549	lung:	n/a
27	chr3:21793557-21793607	HIPEpiC	eye:	n/a
28	chr3:21790232-21790282	HCM	heart:	n/a
29	chr3:21792938-21792988	SKMC	muscle:	n/a
30	chr3:21792434-21792484	NT2-D1	testis:	n/a
31	chr3:21792543-21792593	ovcar-3	ovarian:	n/a
32	chr3:21792857-21792907	HUVEC	blood vessel:	n/a
33	chr3:21792543-21792593	CMK	blood:	n/a
34	chr3:21792965-21793015	HCF	heart:	n/a
35	chr3:21793557-21793607	HepG2	liver:	n/a
36	chr3:21792248-21792298	HRCEpiC	kidney:	n/a
37	chr3:21792543-21792593	SK-N-SH	brain:	n/a
38	chr3:21792434-21792484	HepG2	liver:	n/a
39	chr3:21792938-21792988	GM06990	blood:	n/a
40	chr3:21792684-21792734	HRE	kidney:	n/a
41	chr3:21792434-21792484	GM12878	blood:	n/a
42	chr3:21792434-21792484	MCF-7	breast:	n/a
43	chr3:21792543-21792593	H1-hESC	embryonic stem cell:	embryo
44	chr3:21792857-21792907	HIPEpiC	eye:	n/a
45	chr3:21792965-21793015	ProgFib	skin:	n/a
46	chr3:21792543-21792593	NB4	blood:	n/a
47	chr3:21792965-21793015	HL-60	blood:	n/a
48	chr3:21792248-21792298	LNCaP	prostate:	n/a
49	chr3:21793557-21793607	AG04450	lung:	fetal
50	chr3:21792938-21792988	NHDF-neo	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:21793963..21794585-chr3:21876272..21877179,2	MCF-7	breast:
2	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
3	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF385D	TF binding region
ZNF385D	CpG island

Extended variants
information (count: 1129 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17620313	chr3:21781727-21781728	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11718397	chr3:21781737-21781738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558195489	chr3:21781799-21781800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs576551134	chr3:21781804-21781805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534294551	chr3:21781816-21781817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552965458	chr3:21781903-21781904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79209546	chr3:21781919-21781920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116610369	chr3:21781951-21781952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs137945119	chr3:21781957-21781958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1996630	chr3:21781971-21781972	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs546437860	chr3:21781974-21781975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143502193	chr3:21781994-21781995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs386659205	chr3:21782078-21782079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189496220	chr3:21782088-21782089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181802693	chr3:21782119-21782120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562153818	chr3:21782134-21782135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529274606	chr3:21782141-21782142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116483965	chr3:21782162-21782163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs11711566	chr3:21782164-21782165	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559894793	chr3:21782173-21782174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377595102	chr3:21782184-21782185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536821878	chr3:21782191-21782192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369330610	chr3:21782234-21782235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143935799	chr3:21782240-21782241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73822035	chr3:21782250-21782251	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs76837680	chr3:21782255-21782256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552688537	chr3:21782260-21782261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574331074	chr3:21782264-21782265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79849617	chr3:21782270-21782271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531823788	chr3:21782311-21782312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34859206	chr3:21782313-21782314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369061606	chr3:21782315-21782316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557656692	chr3:21782337-21782338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576031984	chr3:21782348-21782349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546398839	chr3:21782349-21782350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73822036	chr3:21782393-21782394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs114542813	chr3:21782403-21782404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540769673	chr3:21782409-21782410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6784231	chr3:21782411-21782412	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529251416	chr3:21782417-21782418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs185216479	chr3:21782463-21782464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73048207	chr3:21782464-21782465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs148642277	chr3:21782478-21782479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369748895	chr3:21782481-21782482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530745520	chr3:21782520-21782521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143455877	chr3:21782549-21782550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs398105670	chr3:21782550-21782551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs55801703	chr3:21782561-21782562	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs554599165	chr3:21782576-21782577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570357409	chr3:21782582-21782583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21772200-21782400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:21776600-21788800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:21778200-21787800	Weak transcription	Fetal Stomach	stomach
4	chr3:21778200-21791400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:21779200-21784800	Weak transcription	Fetal Muscle Leg	muscle
6	chr3:21780600-21791400	Weak transcription	Fetal Heart	heart
7	chr3:21781000-21788600	Weak transcription	Right Ventricle	heart
8	chr3:21781000-21788800	Weak transcription	Left Ventricle	heart
9	chr3:21781600-21783600	Weak transcription	Aorta	Aorta
10	chr3:21781600-21784200	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr3:21781600-21786600	Weak transcription	Fetal Brain Male	brain
12	chr3:21781800-21782400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:21782400-21782600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr3:21782400-21783000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:21783000-21786400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr3:21783600-21784000	Enhancers	Aorta	Aorta
17	chr3:21784000-21784200	Active TSS	Fetal Muscle Trunk	muscle
18	chr3:21784000-21785000	Weak transcription	Aorta	Aorta
19	chr3:21784200-21785000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr3:21784200-21790600	Weak transcription	Fetal Muscle Trunk	muscle
21	chr3:21784800-21785400	ZNF genes & repeats	Fetal Muscle Leg	muscle
22	chr3:21785000-21785200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr3:21785000-21785200	Enhancers	Aorta	Aorta
24	chr3:21785000-21786400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:21785200-21785600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr3:21785200-21785600	Active TSS	Aorta	Aorta
27	chr3:21785400-21786000	Weak transcription	Fetal Muscle Leg	muscle
28	chr3:21785600-21786400	Weak transcription	Aorta	Aorta
29	chr3:21785600-21787000	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr3:21786000-21786200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr3:21786000-21787000	Enhancers	Fetal Muscle Leg	muscle
32	chr3:21786400-21786600	Enhancers	Right Atrium	heart
33	chr3:21786400-21786600	Enhancers	HMEC	breast
34	chr3:21786400-21787000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr3:21786400-21787000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr3:21786400-21787000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:21786400-21787800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:21786400-21788000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr3:21786400-21789600	Enhancers	Fetal Kidney	kidney
40	chr3:21786400-21789800	Enhancers	NH-A	brain
41	chr3:21786400-21793600	Active TSS	Aorta	Aorta
42	chr3:21786600-21786800	Enhancers	NHDF-Ad	bronchial
43	chr3:21786600-21787000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr3:21786600-21787200	Enhancers	Fetal Brain Male	brain
45	chr3:21786600-21788600	Weak transcription	Right Atrium	heart
46	chr3:21786600-21790000	Enhancers	Fetal Lung	lung
47	chr3:21786800-21787000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:21786800-21787000	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr3:21786800-21787000	Enhancers	HSMMtube	muscle
50	chr3:21786800-21787000	Flanking Active TSS	NHDF-Ad	bronchial

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