Variant report

Variant	rs201234688
Chromosome Location	chr9:117026648-117026649
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr9:117026540-117026676	GM10266	blood:	n/a	n/a
2	CTCF	chr9:117026525-117026658	GM12878	blood:	n/a	n/a
3	CTCF	chr9:117026540-117026690	HepG2	liver:	n/a	n/a
4	CTCF	chr9:117026550-117026656	HepG2	liver:	n/a	n/a
5	CTCF	chr9:117026520-117026670	RPTEC	kidney:	n/a	n/a
6	RAD21	chr9:117026418-117026761	HepG2	liver:	n/a	n/a
7	CTCF	chr9:117026540-117026690	HPF	lung:	n/a	n/a
8	CTCF	chr9:117026435-117026657	K562	blood:	n/a	n/a
9	CTCF	chr9:117026520-117026670	Caco-2	colon:	n/a	n/a
10	CTCF	chr9:117026560-117026710	HEK293	kidney:	n/a	n/a
11	RAD21	chr9:117026498-117026653	K562	blood:	n/a	n/a
12	CTCF	chr9:117026500-117026650	AG10803	skin:	n/a	n/a
13	TBP	chr9:117026647-117026784	H1-hESC	embryonic stem cell:	n/a	n/a
14	RAD21	chr9:117026329-117026802	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:117026500-117026650	HA-sp	spinal cord:	n/a	n/a
16	MAZ	chr9:117026306-117026767	IMR90	lung:	n/a	chr9:117026513-117026523 chr9:117026561-117026571
17	CTCF	chr9:117026500-117026650	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr9:117026520-117026670	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr9:117026540-117026690	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr9:117026520-117026670	HCPEpiC	choroid plexus:	n/a	n/a
21	MAZ	chr9:117026381-117026769	K562	blood:	n/a	chr9:117026513-117026523 chr9:117026561-117026571
22	CTCF	chr9:117026536-117026660	GM19238	blood:	n/a	n/a
23	CTCF	chr9:117026520-117026670	HepG2	liver:	n/a	n/a
24	CTCF	chr9:117026500-117026650	HCM	heart:	n/a	n/a
25	CTCF	chr9:117026620-117026770	A549	lung:	n/a	n/a
26	RAD21	chr9:117026323-117026860	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:117026503-117026698	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:117026540-117026690	AG09319	gingival:	n/a	n/a
29	CTCF	chr9:117026559-117026670	GM13977	blood:	n/a	n/a
30	RAD21	chr9:117026418-117026765	IMR90	lung:	n/a	n/a
31	CTCF	chr9:117026477-117026700	K562	blood:	n/a	n/a
32	RAD21	chr9:117026414-117026670	HepG2	liver:	n/a	n/a
33	CTCF	chr9:117026520-117026670	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr9:117026500-117026650	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr9:117026520-117026670	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr9:117026459-117026700	K562	blood:	n/a	n/a
37	RAD21	chr9:117026419-117026782	ECC-1	luminal epithelium:	n/a	n/a
38	CTCF	chr9:117026580-117026730	GM12871	blood:	n/a	n/a
39	CTCF	chr9:117026527-117026701	Medullo	brain:	n/a	n/a
40	SMC3	chr9:117026418-117026733	K562	blood:	n/a	chr9:117026568-117026576
41	CTCF	chr9:117026529-117026666	GM12892	blood:	n/a	n/a
42	CTCF	chr9:117026500-117026650	GM06990	blood:	n/a	n/a
43	CTCF	chr9:117026520-117026670	HMF	breast:	n/a	n/a
44	CTCF	chr9:117026412-117026662	A549	lung:	n/a	n/a
45	CTCF	chr9:117026520-117026670	K562	blood:	n/a	n/a
46	SIN3A	chr9:117026555-117026667	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr9:117026580-117026730	HFF	foreskin:	n/a	n/a
48	CTCF	chr9:117026524-117026652	GM12891	blood:	n/a	n/a
49	RAD21	chr9:117026322-117026828	HCT-116	colon:	n/a	n/a
50	ZNF143	chr9:117026459-117026659	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr9:117019506..117021498-chr9:117026111..117027904,2	MCF-7	breast:
2	chr9:116869905..116870808-chr9:117026020..117026989,3	MCF-7	breast:
3	chr9:116844543..116845536-chr9:117026114..117026681,2	K562	blood:
4	chr9:116869941..116870862-chr9:117026162..117027038,2	K562	blood:

No data

Variant related genes	Relation type
COL27A1	TF binding region

Extended variants
information (count: 39 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430093	chr9:116330446-117325446	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	esv2422396	chr9:116792944-117354862	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
3	esv2422492	chr9:116811294-117366643	Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
4	esv2761285	chr9:116811897-117103268	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
5	nsv870215	chr9:116842614-117070344	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	124 gene(s)	inside rSNPs	diseases
6	nsv466533	chr9:116930100-117248479	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	128 gene(s)	inside rSNPs	diseases
7	nsv615233	chr9:116930100-117248479	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	128 gene(s)	inside rSNPs	diseases
8	nsv1051544	chr9:116944940-117443031	ZNF genes & repeats Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
9	nsv540203	chr9:116944940-117443031	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
10	nsv1048093	chr9:116945025-117456210	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
11	nsv1050991	chr9:116953739-117442999	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
12	nsv1046311	chr9:116953739-117447142	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
13	nsv1052877	chr9:116953739-117456210	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
14	nsv1039681	chr9:116953739-117457158	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
15	nsv1051987	chr9:116955841-117453668	Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
16	nsv1044374	chr9:116955841-117460150	Genic enhancers Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
17	nsv466534	chr9:116956268-117455810	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
18	nsv615234	chr9:116956268-117455810	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
19	nsv1048817	chr9:116957958-117456210	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
20	nsv615235	chr9:116958144-117367061	ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
21	nsv615236	chr9:116958144-117455810	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
22	nsv466535	chr9:116958144-117456175	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
23	nsv615237	chr9:116958144-117456175	Strong transcription Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
24	nsv615238	chr9:116958144-117458475	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
25	nsv430094	chr9:116958446-117456446	Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
26	nsv1053756	chr9:116975934-117443031	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
27	nsv540204	chr9:116975934-117443031	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
28	nsv1047704	chr9:116978041-117399362	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
29	nsv540205	chr9:116978041-117399362	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
30	esv1840888	chr9:116983847-117047121	Genic enhancers Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
31	nsv530950	chr9:117009156-117399361	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
32	nsv916139	chr9:117009169-117399454	Weak transcription Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
33	nsv1047822	chr9:117010663-117211517	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
34	nsv893753	chr9:117015956-117028506	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
35	nsv893754	chr9:117015956-117099995	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
36	nsv893755	chr9:117019801-117032189	Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
37	nsv893756	chr9:117019801-117056851	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
38	nsv893757	chr9:117021374-117120680	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
39	esv3415028	chr9:117026522-117026684	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116973400-117047000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:116978600-117041200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:116978800-117027600	Weak transcription	Esophagus	oesophagus
4	chr9:116978800-117027600	Weak transcription	Gastric	stomach
5	chr9:116999800-117034600	Weak transcription	HMEC	breast
6	chr9:117001600-117039400	Weak transcription	HUVEC	blood vessel
7	chr9:117002000-117041000	Weak transcription	Aorta	Aorta
8	chr9:117002800-117027000	Weak transcription	Spleen	Spleen
9	chr9:117005000-117050200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:117008600-117029000	Weak transcription	NHEK	skin
11	chr9:117011800-117030000	Strong transcription	HepG2	liver
12	chr9:117012400-117054400	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:117013200-117028600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:117013200-117028800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:117013200-117028800	Weak transcription	HSMM	muscle
16	chr9:117013200-117029200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr9:117013200-117033600	Weak transcription	NHLF	lung
18	chr9:117013400-117027000	Weak transcription	Pancreas	Pancrea
19	chr9:117013400-117039400	Weak transcription	Ovary	ovary
20	chr9:117013400-117067800	Weak transcription	Right Ventricle	heart
21	chr9:117013600-117027000	Weak transcription	Lung	lung
22	chr9:117014200-117038400	Weak transcription	NHDF-Ad	bronchial
23	chr9:117015400-117037600	Weak transcription	A549	lung
24	chr9:117016200-117047400	Weak transcription	Fetal Kidney	kidney
25	chr9:117016800-117039400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr9:117017600-117027600	Genic enhancers	Fetal Muscle Trunk	muscle
27	chr9:117019400-117027800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:117019800-117029000	Weak transcription	HSMMtube	muscle
29	chr9:117020800-117037800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr9:117022400-117038600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:117023600-117027200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:117024000-117027200	Weak transcription	Colon Smooth Muscle	Colon
33	chr9:117024200-117033600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr9:117024400-117027400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr9:117024600-117033800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr9:117024600-117037600	Weak transcription	Stomach Mucosa	stomach
37	chr9:117024800-117028600	Weak transcription	Left Ventricle	heart
38	chr9:117024800-117033600	Weak transcription	Colonic Mucosa	Colon
39	chr9:117024800-117043000	Weak transcription	Right Atrium	heart
40	chr9:117025400-117026800	Genic enhancers	Fetal Stomach	stomach
41	chr9:117025600-117027600	Genic enhancers	Fetal Muscle Leg	muscle
42	chr9:117025800-117027200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr9:117025800-117027400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:117025800-117027600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr9:117025800-117028600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:117026000-117026800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr9:117026000-117027000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr9:117026000-117041800	Strong transcription	Liver	Liver
49	chr9:117026200-117026800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
50	chr9:117026200-117026800	Genic enhancers	Fetal Intestine Large	intestine

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