Variant report

Variant	nsv615227
Chromosome Location	chr9:116904534-116924781
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	chr9:116917556-116917812	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116916117-116916350	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:116904220-116904556	HepG2	liver:	n/a	n/a
4	BACH1	chr9:116919190-116919252	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:116916262-116917825	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:116918832-116918950	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr9:116916072-116916459	HepG2	liver:	n/a	chr9:116916326-116916342
8	BHLHE40	chr9:116916169-116916429	HepG2	liver:	n/a	chr9:116916326-116916342
9	BHLHE40	chr9:116917582-116917706	K562	blood:	n/a	n/a
10	BHLHE40	chr9:116916046-116916890	HepG2	liver:	n/a	chr9:116916562-116916578 chr9:116916504-116916520 chr9:116916326-116916342
11	BHLHE40	chr9:116917652-116917813	GM12878	blood:	n/a	n/a
12	BRCA1	chr9:116916125-116916314	HepG2	liver:	n/a	n/a
13	BRCA1	chr9:116917608-116917881	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr9:116917603-116917846	K562	blood:	n/a	n/a
15	CEBPB	chr9:116920204-116920447	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:116917574-116917748	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:116918614-116918817	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:116918582-116919517	IMR90	lung:	n/a	n/a
19	CEBPB	chr9:116917541-116917736	HepG2	liver:	n/a	n/a
20	CEBPD	chr9:116916078-116916534	HepG2	liver:	n/a	n/a
21	CHD1	chr9:116917619-116917971	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD1	chr9:116917409-116920757	IMR90	lung:	n/a	n/a
23	CHD2	chr9:116917730-116917764	GM12878	blood:	n/a	n/a
24	CHD2	chr9:116917633-116917951	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr9:116917641-116917827	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr9:116916895-116917095	HepG2	liver:	n/a	n/a
27	CHD2	chr9:116916123-116916384	HepG2	liver:	n/a	chr9:116916326-116916336
28	CREB1	chr9:116917536-116918110	A549	lung:	n/a	n/a
29	CTBP2	chr9:116918708-116919951	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTBP2	chr9:116915982-116917075	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr9:116917548-116918440	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr9:116917620-116917770	GM12878	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
33	CTCF	chr9:116916120-116916270	AG04450	lung:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
34	CTCF	chr9:116916080-116916230	WI-38	lung:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
35	CTCF	chr9:116915804-116916550	SK-N-SH	brain:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
36	CTCF	chr9:116919057-116919268	Fibrobl	skin:	n/a	n/a
37	CTCF	chr9:116916080-116916230	RPTEC	kidney:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
38	CTCF	chr9:116916100-116916250	NHEK	skin:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
39	CTCF	chr9:116916120-116916270	HBMEC	blood vessel:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
40	CTCF	chr9:116916140-116916254	LNCaP	prostate:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
41	CTCF	chr9:116915992-116916405	A549	lung:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
42	CTCF	chr9:116919120-116919270	AG04449	skin:	n/a	n/a
43	CTCF	chr9:116917494-116917909	K562	blood:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
44	CTCF	chr9:116916072-116916285	MCF-7	breast:	n/a	chr9:116916166-116916179 chr9:116916164-116916182
45	CTCF	chr9:116919060-116919210	HCM	heart:	n/a	n/a
46	CTCF	chr9:116917640-116917790	AoAF	blood vessel:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
47	CTCF	chr9:116917580-116917730	GM12872	blood:	n/a	chr9:116917702-116917720 chr9:116917715-116917728 chr9:116917712-116917730 chr9:116917705-116917718
48	CTCF	chr9:116917680-116917830	HCM	heart:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718
49	CTCF	chr9:116917180-116917330	GM12871	blood:	n/a	n/a
50	CTCF	chr9:116917640-116917790	Caco-2	colon:	n/a	chr9:116917702-116917720 chr9:116917722-116917740 chr9:116917715-116917728 chr9:116917725-116917738 chr9:116917712-116917730 chr9:116917705-116917718

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116917393-116917443	HCT-116	colon:	n/a
2	chr9:116918183-116918233	HEK293	kidney:	embryo
3	chr9:116917393-116917443	AG04450	lung:	fetal
4	chr9:116918477-116918527	HCPEpiC	choroid plexus:	n/a
5	chr9:116917393-116917443	U87	brain:	n/a
6	chr9:116918247-116918297	BE2_C	brain:	n/a
7	chr9:116917393-116917443	MCF10A-Er-Src	breast:	n/a
8	chr9:116918247-116918297	HEEpiC	esophagus:	n/a
9	chr9:116918183-116918233	Jurkat	blood:	n/a
10	chr9:116918183-116918233	SK-N-SH_RA	brain:	n/a
11	chr9:116918183-116918233	BJ	skin:	n/a
12	chr9:116918183-116918233	HUVEC	blood vessel:	n/a
13	chr9:116918247-116918297	CMK	blood:	n/a
14	chr9:116918183-116918233	Hela-S3	cervix:	n/a
15	chr9:116916031-116916081	SKMC	muscle:	n/a
16	chr9:116914074-116914124	A549	lung:	n/a
17	chr9:116918247-116918297	LNCaP	prostate:	n/a
18	chr9:116916031-116916081	PrEC	prostate:	n/a
19	chr9:116916031-116916081	Jurkat	blood:	n/a
20	chr9:116916031-116916081	ProgFib	skin:	n/a
21	chr9:116916031-116916081	MCF10A-Er-Src	breast:	n/a
22	chr9:116918183-116918233	GM12878	blood:	n/a
23	chr9:116918247-116918297	Jurkat	blood:	n/a
24	chr9:116918477-116918527	A549	lung:	n/a
25	chr9:116918183-116918233	HL-60	blood:	n/a
26	chr9:116916031-116916081	GM19239	blood:	n/a
27	chr9:116916031-116916081	HUVEC	blood vessel:	n/a
28	chr9:116918183-116918233	HCM	heart:	n/a
29	chr9:116914074-116914124	BE2_C	brain:	n/a
30	chr9:116917393-116917443	ovcar-3	ovarian:	n/a
31	chr9:116914074-116914124	RPTEC	kidney:	n/a
32	chr9:116918477-116918527	HAEpiC	amniotic membrane:	n/a
33	chr9:116917393-116917443	HRPEpiC	eye:	n/a
34	chr9:116916031-116916081	H1-hESC	embryonic stem cell:	embryo
35	chr9:116914074-116914124	AG09319	gingival:	n/a
36	chr9:116918183-116918233	MCF10A-Er-Src	breast:	n/a
37	chr9:116917393-116917443	HMEC	breast:	n/a
38	chr9:116914074-116914124	AG09309	skin:	n/a
39	chr9:116917393-116917443	HAEpiC	amniotic membrane:	n/a
40	chr9:116918247-116918297	HAEpiC	amniotic membrane:	n/a
41	chr9:116916031-116916081	HCT-116	colon:	n/a
42	chr9:116918183-116918233	HPAEpiC	pulmonary alveolar:	n/a
43	chr9:116918477-116918527	PrEC	prostate:	n/a
44	chr9:116918247-116918297	HRPEpiC	eye:	n/a
45	chr9:116918247-116918297	GM12878	blood:	n/a
46	chr9:116918477-116918527	Caco-2	colon:	n/a
47	chr9:116917393-116917443	SK-N-MC	brain:	n/a
48	chr9:116914074-116914124	NH-A	brain:	n/a
49	chr9:116918477-116918527	RPTEC	kidney:	n/a
50	chr9:116918477-116918527	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:116869891..116870803-chr9:116915238..116916605,3	MCF-7	breast:
2	chr9:116915372..116918710-chr9:116920861..116924845,3	MCF-7	breast:
3	chr9:116846273..116847216-chr9:116922173..116922681,2	MCF-7	breast:
4	chr9:116918121..116920168-chr9:116937255..116940070,3	K562	blood:
5	chr9:116903323..116904967-chr9:116908753..116911536,2	K562	blood:
6	chr9:116906533..116909775-chr9:116912915..116915543,3	MCF-7	breast:
7	chr9:116869949..116870838-chr9:116915614..116916621,9	MCF-7	breast:
8	chr9:116909854..116913482-chr9:116913961..116916713,3	MCF-7	breast:
9	chr9:116901825..116904823-chr9:116906598..116910253,3	K562	blood:
10	chr9:116918924..116921858-chr9:116922744..116925296,3	K562	blood:
11	chr9:116903323..116904967-chr9:116908753..116911536,2	K562	blood:
12	chr9:116894422..116897805-chr9:116912339..116915406,3	MCF-7	breast:
13	chr9:116870237..116871907-chr9:116924776..116927376,2	MCF-7	breast:
14	chr9:116906533..116909775-chr9:116912915..116915543,3	MCF-7	breast:
15	chr9:116909854..116913482-chr9:116913961..116916713,3	MCF-7	breast:
16	chr9:116922253..116925161-chr9:116948030..116950142,2	MCF-7	breast:
17	chr9:116917422..116918284-chr9:117067805..117069207,4	K562	blood:
18	chr9:116918924..116921858-chr9:116922744..116925296,3	K562	blood:
19	chr9:116914824..116917398-chr9:116971543..116973662,2	MCF-7	breast:
20	chr9:116899310..116902540-chr9:116902912..116904896,4	K562	blood:
21	chr9:116901825..116904823-chr9:116906598..116910253,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF12-2	chr9:116914873-116914992	NONHSAT134368
2	lnc-KIF12-2	chr9:116906868-116907335	NONHSAT134368
3	lnc-KIF12-3	chr9:116921639-116921808	NONHSAT134369
4	lnc-KIF12-2	chr9:116908781-116909341	NONHSAT134368

Variant related genes	Relation type
COL27A1	TF binding region
COL27A1	CpG island
ENSG00000196739	chromatin interactions
ENSG00000207726	chromatin interactions

Extended variants
information (count: 749 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:749 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2043195	chr9:116904534-116904535	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs188168628	chr9:116904540-116904541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs529764840	chr9:116904563-116904564	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs372580799	chr9:116904607-116904608	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs546631026	chr9:116904673-116904674	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs566476896	chr9:116904695-116904696	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs532141231	chr9:116904719-116904720	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs55922812	chr9:116904747-116904748	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs569554900	chr9:116904757-116904758	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs538504337	chr9:116904762-116904763	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs528386347	chr9:116904764-116904765	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs540161812	chr9:116904790-116904791	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs565052604	chr9:116904797-116904798	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs534038416	chr9:116904798-116904799	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs553849157	chr9:116904818-116904819	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575350948	chr9:116904912-116904913	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576869946	chr9:116904922-116904923	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532224397	chr9:116905038-116905039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553091255	chr9:116905057-116905058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs550821116	chr9:116905063-116905064	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545778676	chr9:116905071-116905072	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558454755	chr9:116905084-116905085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575468787	chr9:116905090-116905091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544458436	chr9:116905212-116905213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560931960	chr9:116905234-116905235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529847717	chr9:116905261-116905262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79553480	chr9:116905273-116905274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78902542	chr9:116905274-116905275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540375880	chr9:116905278-116905279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144904411	chr9:116905311-116905312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532177896	chr9:116905330-116905331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539303684	chr9:116905342-116905343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552179145	chr9:116905373-116905374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558078231	chr9:116905401-116905402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531923659	chr9:116905402-116905403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs573212092	chr9:116905404-116905405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568609761	chr9:116905405-116905406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540211986	chr9:116905406-116905407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534397974	chr9:116905424-116905425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547521130	chr9:116905425-116905426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529853338	chr9:116905447-116905448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548203071	chr9:116905450-116905451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539517637	chr9:116905456-116905457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556152460	chr9:116905496-116905497	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566347888	chr9:116905498-116905499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576342847	chr9:116905505-116905506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537750760	chr9:116905539-116905540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4979341	chr9:116905543-116905544	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs145726211	chr9:116905548-116905549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553404427	chr9:116905549-116905550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	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
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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116892800-116916000	Weak transcription	Gastric	stomach
2	chr9:116900600-116904600	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr9:116900800-116905000	Enhancers	Left Ventricle	heart
4	chr9:116900800-116905200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr9:116900800-116906200	Enhancers	HepG2	liver
6	chr9:116901200-116905000	Enhancers	Fetal Lung	lung
7	chr9:116901800-116904800	Enhancers	Fetal Heart	heart
8	chr9:116901800-116904800	Enhancers	Ovary	ovary
9	chr9:116901800-116905000	Enhancers	Right Atrium	heart
10	chr9:116902200-116906000	Enhancers	Fetal Stomach	stomach
11	chr9:116902400-116905600	Enhancers	HSMMtube	muscle
12	chr9:116902600-116904800	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr9:116902600-116907800	Enhancers	Fetal Muscle Leg	muscle
14	chr9:116902800-116904800	Enhancers	Psoas Muscle	Psoas
15	chr9:116903000-116904600	Enhancers	Fetal Intestine Small	intestine
16	chr9:116903000-116904600	Enhancers	Rectal Smooth Muscle	rectum
17	chr9:116903200-116904600	Weak transcription	Lung	lung
18	chr9:116903400-116904800	Enhancers	Liver	Liver
19	chr9:116903400-116904800	Enhancers	Colon Smooth Muscle	Colon
20	chr9:116903400-116904800	Enhancers	Fetal Intestine Large	intestine
21	chr9:116903400-116904800	Enhancers	Right Ventricle	heart
22	chr9:116903400-116905800	Enhancers	Fetal Muscle Trunk	muscle
23	chr9:116903800-116904600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
24	chr9:116903800-116904600	Enhancers	Brain Substantia Nigra	brain
25	chr9:116903800-116904600	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr9:116903800-116904800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr9:116903800-116904800	Enhancers	Pancreas	Pancrea
28	chr9:116903800-116905000	Enhancers	Adipose Nuclei	Adipose
29	chr9:116903800-116905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr9:116903800-116905000	Enhancers	Stomach Mucosa	stomach
31	chr9:116904000-116904600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:116904200-116904600	Enhancers	Duodenum Mucosa	Duodenum
33	chr9:116904400-116904600	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
34	chr9:116904400-116904600	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr9:116904400-116905000	Bivalent Enhancer	Placenta	Placenta
36	chr9:116904600-116904800	Enhancers	Lung	lung
37	chr9:116904600-116904800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr9:116904600-116904800	Enhancers	Stomach Smooth Muscle	stomach
39	chr9:116904800-116905600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr9:116905200-116905600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr9:116905600-116905800	Bivalent Enhancer	HSMMtube	muscle
42	chr9:116905600-116906000	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr9:116906200-116906400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr9:116906200-116908200	Weak transcription	HepG2	liver
45	chr9:116906600-116910800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr9:116907600-116908400	Bivalent Enhancer	Placenta	Placenta
47	chr9:116907800-116908000	Enhancers	Right Ventricle	heart
48	chr9:116907800-116908800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:116908000-116916000	Weak transcription	Right Ventricle	heart
50	chr9:116908200-116908800	Enhancers	HepG2	liver

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