Variant report

Variant	nsv982544
Chromosome Location	chr9:95644425-95647585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr9:95644651-95644836	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr9:95644664-95644871	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr9:95646440-95646590	HepG2	liver:	n/a	n/a
4	CTCF	chr9:95646320-95646470	HA-sp	spinal cord:	n/a	n/a
5	CTCF	chr9:95646342-95646343	K562	blood:	n/a	n/a
6	CTCF	chr9:95646460-95646610	HCM	heart:	n/a	n/a
7	CTCF	chr9:95646080-95646230	K562	blood:	n/a	n/a
8	CTCF	chr9:95646340-95646490	GM12874	blood:	n/a	n/a
9	CTCF	chr9:95646441-95646473	HUVEC	blood vessel:	n/a	n/a
10	CTCF	chr9:95646440-95646590	GM12864	blood:	n/a	n/a
11	CTCF	chr9:95646460-95646610	GM12869	blood:	n/a	n/a
12	CTCF	chr9:95646306-95646569	K562	blood:	n/a	n/a
13	CTCF	chr9:95646400-95646550	GM12871	blood:	n/a	n/a
14	CTCF	chr9:95646380-95646530	GM12873	blood:	n/a	n/a
15	CTCF	chr9:95646380-95646530	GM12872	blood:	n/a	n/a
16	CTCF	chr9:95646040-95646190	WI-38	lung:	n/a	n/a
17	CTCF	chr9:95646378-95646501	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr9:95646440-95646590	K562	blood:	n/a	n/a
19	CTCF	chr9:95646460-95646610	HMEC	breast:	n/a	n/a
20	CTCF	chr9:95646418-95646568	GM19239	blood:	n/a	n/a
21	CTCF	chr9:95646467-95646488	ProgFib	skin:	n/a	n/a
22	CTCF	chr9:95646394-95646549	MCF-7	breast:	n/a	n/a
23	CTCF	chr9:95646520-95646670	A549	lung:	n/a	n/a
24	CTCF	chr9:95646580-95646730	GM12868	blood:	n/a	n/a
25	CTCF	chr9:95646440-95646590	GM12872	blood:	n/a	n/a
26	CTCF	chr9:95646340-95646490	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr9:95646286-95646571	K562	blood:	n/a	n/a
28	CTCF	chr9:95646500-95646650	MCF-7	breast:	n/a	n/a
29	CTCF	chr9:95646379-95646525	GM19238	blood:	n/a	n/a
30	CTCF	chr9:95646400-95646550	GM12864	blood:	n/a	n/a
31	CTCF	chr9:95646402-95646485	Lung_OC	lung:	n/a	n/a
32	CTCF	chr9:95646480-95646630	GM12873	blood:	n/a	n/a
33	CTCF	chr9:95646440-95646590	GM12873	blood:	n/a	n/a
34	CTCF	chr9:95646440-95646590	HEK293	kidney:	n/a	n/a
35	CTCF	chr9:95646294-95646530	K562	blood:	n/a	n/a
36	CTCF	chr9:95646412-95646530	GM10266	blood:	n/a	n/a
37	CTCF	chr9:95646417-95646501	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr9:95646383-95646558	GM13977	blood:	n/a	n/a
39	CTCF	chr9:95646405-95646530	GM12892	blood:	n/a	n/a
40	CTCF	chr9:95646460-95646610	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr9:95646414-95646525	HepG2	liver:	n/a	n/a
42	CTCF	chr9:95646436-95646458	Medullo	brain:	n/a	n/a
43	CTCF	chr9:95646440-95646590	HMF	breast:	n/a	n/a
44	CTCF	chr9:95646480-95646630	K562	blood:	n/a	n/a
45	CTCF	chr9:95646480-95646630	HepG2	liver:	n/a	n/a
46	CTCF	chr9:95646480-95646630	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr9:95646544-95646650	GM20000	blood:	n/a	n/a
48	CTCF	chr9:95646120-95646270	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr9:95646394-95646507	GM12878	blood:	n/a	n/a
50	CTCF	chr9:95647281-95647383	GM13976	blood:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95632175..95634114-chr9:95643076..95644693,2	K562	blood:
2	chr9:95644477..95647026-chr9:95856409..95858869,2	MCF-7	breast:
3	chr9:95630810..95632810-chr9:95646965..95649484,2	MCF-7	breast:
4	chr9:95638865..95641445-chr9:95646989..95649985,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGD3-3	chr9:95646188-95646282	NONHSAT133210
2	lnc-FGD3-3	chr9:95647164-95647333	NONHSAT133209
3	lnc-FGD3-3	chr9:95646467-95646908	NONHSAT133213
4	lnc-FGD3-3	chr9:95646193-95646282	NONHSAT133212
5	lnc-FGD3-3	chr9:95644865-95645071	NONHSAT133210
6	lnc-FGD3-3	chr9:95647164-95648440	NONHSAT133213
7	lnc-FGD3-3	chr9:95646188-95646282	NONHSAT133209
8	lnc-FGD3-3	chr9:95646848-95646908	NONHSAT133212
9	lnc-FGD3-3	chr9:95646848-95646908	NONHSAT133210
10	lnc-FGD3-3	chr9:95646848-95646908	NONHSAT133209
11	lnc-FGD3-3	chr9:95644849-95645071	NONHSAT133209

No data

Variant related genes	Relation type
ENSG00000226668	TF binding region
ZNF484	TF binding region
ENSG00000127081	chromatin interactions
ENSG00000223446	chromatin interactions
ENSG00000165233	chromatin interactions

Extended variants
information (count: 173 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:173 , 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	rs187048016	chr9:95644426-95644427	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs551254274	chr9:95644432-95644433	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs12342474	chr9:95644434-95644435	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533760424	chr9:95644436-95644437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs191459225	chr9:95644441-95644442	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs182098784	chr9:95644467-95644468	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs567322116	chr9:95644509-95644510	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs537569265	chr9:95644523-95644524	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540360722	chr9:95644542-95644543	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560455137	chr9:95644605-95644606	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs556672709	chr9:95644611-95644612	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs578225149	chr9:95644616-95644617	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs138105762	chr9:95644623-95644624	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs554500094	chr9:95644705-95644706	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs374991841	chr9:95644714-95644715	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs542989664	chr9:95644733-95644734	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs142699419	chr9:95644736-95644737	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs576454322	chr9:95644738-95644739	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs369118727	chr9:95644739-95644740	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs201539435	chr9:95644766-95644767	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs41273380	chr9:95644791-95644792	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs41273382	chr9:95644808-95644809	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs145937412	chr9:95644830-95644831	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs41273384	chr9:95644836-95644837	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138553198	chr9:95644838-95644839	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs569536369	chr9:95644855-95644856	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs187851448	chr9:95644861-95644862	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs2296059	chr9:95644873-95644874	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537909095	chr9:95644888-95644889	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs149246610	chr9:95644919-95644920	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs571410743	chr9:95644927-95644928	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
32	rs551966261	chr9:95644936-95644937	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs193140939	chr9:95644951-95644952	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs7854940	chr9:95644970-95644971	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185612454	chr9:95644992-95644993	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs148433406	chr9:95644994-95644995	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs576368523	chr9:95645005-95645006	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs2296060	chr9:95645020-95645021	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs565016460	chr9:95645021-95645022	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs576959876	chr9:95645029-95645030	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs544771114	chr9:95645031-95645032	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs559939550	chr9:95645038-95645039	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs527536003	chr9:95645039-95645040	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs549019100	chr9:95645041-95645042	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs561278497	chr9:95645056-95645057	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs558223886	chr9:95645060-95645061	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs531202885	chr9:95645091-95645092	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs190090016	chr9:95645103-95645104	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571347944	chr9:95645110-95645111	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533081505	chr9:95645190-95645191	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95640400-95644600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:95640400-95644800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:95640600-95645000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:95640600-95645800	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr9:95640600-95648800	Weak transcription	Thymus	Thymus
6	chr9:95640800-95644600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:95640800-95644600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr9:95640800-95644800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr9:95640800-95645200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:95640800-95646000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr9:95640800-95646400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr9:95640800-95647800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr9:95640800-95648600	Weak transcription	Primary T cells from cord blood	blood
14	chr9:95640800-95648600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr9:95641000-95646000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr9:95641000-95646600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr9:95641000-95648400	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr9:95644400-95644600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr9:95644400-95645000	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr9:95644400-95645400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr9:95644400-95645400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr9:95644600-95645000	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr9:95644600-95646000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr9:95644600-95646800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr9:95644600-95647200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:95644800-95645600	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr9:95644800-95646400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr9:95645000-95645200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr9:95645000-95645400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr9:95645000-95646400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr9:95645000-95646400	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr9:95645000-95647000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr9:95645200-95645400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
34	chr9:95645200-95647000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr9:95645400-95645600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
36	chr9:95645400-95645600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr9:95645600-95646000	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr9:95645600-95646000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr9:95645800-95646800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
40	chr9:95645800-95646800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr9:95645800-95647200	Enhancers	Primary T cells fromperipheralblood	blood
42	chr9:95646000-95646200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr9:95646000-95646400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr9:95646000-95646600	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr9:95646000-95646600	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr9:95646000-95646600	Enhancers	Fetal Muscle Trunk	muscle
47	chr9:95646200-95646400	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr9:95646200-95646600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr9:95646400-95646800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr9:95646400-95646800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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