Variant report

Variant	esv3366065
Chromosome Location	chr7:39871977-39874075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:131)
CpG islands
(count:183)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:131 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr7:39872998-39873043	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTBP2	chr7:39872920-39873280	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr7:39872996-39873061	A549	lung:	n/a	n/a
4	CTCF	chr7:39872836-39873207	K562	blood:	n/a	n/a
5	CTCF	chr7:39873080-39873230	HRE	kidney:	n/a	n/a
6	CTCF	chr7:39873004-39873132	Fibrobl	skin:	n/a	n/a
7	CTCF	chr7:39872880-39873030	GM12871	blood:	n/a	n/a
8	CTCF	chr7:39873140-39873290	HMEC	breast:	n/a	n/a
9	CTCF	chr7:39872940-39873090	AG04449	skin:	n/a	n/a
10	CTCF	chr7:39874056-39874113	MCF-7	breast:	n/a	n/a
11	CTCF	chr7:39872900-39873050	GM12869	blood:	n/a	n/a
12	CTCF	chr7:39872886-39873115	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr7:39872911-39873054	HepG2	liver:	n/a	n/a
14	CTCF	chr7:39872940-39873090	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr7:39872940-39873090	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr7:39872960-39873110	AG09309	skin:	n/a	n/a
17	CTCF	chr7:39872860-39873010	GM12865	blood:	n/a	n/a
18	CTCF	chr7:39872949-39873205	IMR90	lung:	n/a	n/a
19	CTCF	chr7:39872920-39873070	GM12873	blood:	n/a	n/a
20	CTCF	chr7:39873179-39873216	ProgFib	skin:	n/a	n/a
21	CTCF	chr7:39872980-39873130	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr7:39872888-39873077	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr7:39872942-39873065	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr7:39872961-39873262	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:39873163-39873245	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:39872837-39873109	K562	blood:	n/a	n/a
27	CTCF	chr7:39873163-39873253	Gliobla	brain:	n/a	n/a
28	CTCF	chr7:39872880-39873030	GM12865	blood:	n/a	n/a
29	CTCF	chr7:39872900-39873050	GM12868	blood:	n/a	n/a
30	CTCF	chr7:39872880-39873030	GM12874	blood:	n/a	n/a
31	CTCF	chr7:39872959-39873050	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:39872880-39873030	GM12866	blood:	n/a	n/a
33	CTCF	chr7:39873180-39873330	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:39872939-39873078	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:39872789-39873259	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:39872960-39873110	Caco-2	colon:	n/a	n/a
37	CTCF	chr7:39872900-39873050	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr7:39872920-39873070	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr7:39872984-39873084	GM13977	blood:	n/a	n/a
40	CTCF	chr7:39872860-39873010	HRE	kidney:	n/a	n/a
41	CTCF	chr7:39873099-39873249	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:39872940-39873090	HEK293	kidney:	n/a	n/a
43	CTCF	chr7:39872960-39873110	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr7:39872940-39873090	GM12870	blood:	n/a	n/a
45	CTCF	chr7:39872940-39873090	AG04450	lung:	n/a	n/a
46	CTCF	chr7:39872960-39873110	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr7:39872880-39873030	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr7:39872880-39873030	Caco-2	colon:	n/a	n/a
49	CTCF	chr7:39873016-39873028	Gliobla	brain:	n/a	n/a
50	CTCF	chr7:39872940-39873090	AG09319	gingival:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39873832-39873882	A549	lung:	n/a
2	chr7:39873001-39873051	HNPCEpiC	eye:	n/a
3	chr7:39873001-39873051	AG10803	skin:	n/a
4	chr7:39873001-39873051	GM12878	blood:	n/a
5	chr7:39873001-39873051	HRE	kidney:	n/a
6	chr7:39873001-39873051	HMEC	breast:	n/a
7	chr7:39872851-39872901	AoSMC	blood vessel:	n/a
8	chr7:39873001-39873051	AG04449	skin:	fetal
9	chr7:39872851-39872901	HRCEpiC	kidney:	n/a
10	chr7:39872851-39872901	BJ	skin:	n/a
11	chr7:39873001-39873051	NH-A	brain:	n/a
12	chr7:39873832-39873882	K562	blood:	n/a
13	chr7:39872851-39872901	PFSK-1	brain:	n/a
14	chr7:39873832-39873882	AG10803	skin:	n/a
15	chr7:39872851-39872901	IMR90	lung:	fetal
16	chr7:39873832-39873882	MCF10A-Er-Src	breast:	n/a
17	chr7:39873001-39873051	SKMC	muscle:	n/a
18	chr7:39873832-39873882	SAEC	small airway:	n/a
19	chr7:39873001-39873051	ProgFib	skin:	n/a
20	chr7:39873001-39873051	HUVEC	blood vessel:	n/a
21	chr7:39873832-39873882	HCM	heart:	n/a
22	chr7:39872851-39872901	HMEC	breast:	n/a
23	chr7:39873832-39873882	SK-N-MC	brain:	n/a
24	chr7:39873001-39873051	SK-N-SH	brain:	n/a
25	chr7:39872851-39872901	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:39872851-39872901	AG04450	lung:	fetal
27	chr7:39872851-39872901	GM06990	blood:	n/a
28	chr7:39873001-39873051	LNCaP	prostate:	n/a
29	chr7:39872851-39872901	Hepatocyte	liver:	n/a
30	chr7:39872851-39872901	HIPEpiC	eye:	n/a
31	chr7:39873832-39873882	BE2_C	brain:	n/a
32	chr7:39872851-39872901	NHDF-neo	bronchial:	n/a
33	chr7:39872851-39872901	H1-hESC	embryonic stem cell:	embryo
34	chr7:39873001-39873051	HL-60	blood:	n/a
35	chr7:39873832-39873882	AG04450	lung:	fetal
36	chr7:39872851-39872901	AG09309	skin:	n/a
37	chr7:39873001-39873051	HRCEpiC	kidney:	n/a
38	chr7:39873832-39873882	HRE	kidney:	n/a
39	chr7:39873001-39873051	PFSK-1	brain:	n/a
40	chr7:39873832-39873882	HIPEpiC	eye:	n/a
41	chr7:39872851-39872901	SAEC	small airway:	n/a
42	chr7:39872851-39872901	GM12892	blood:	n/a
43	chr7:39873832-39873882	AG04449	skin:	fetal
44	chr7:39873832-39873882	MCF-7	breast:	n/a
45	chr7:39873832-39873882	AoSMC	blood vessel:	n/a
46	chr7:39873832-39873882	NB4	blood:	n/a
47	chr7:39872851-39872901	ovcar-3	ovarian:	n/a
48	chr7:39873832-39873882	SK-N-SH_RA	brain:	n/a
49	chr7:39873001-39873051	IMR90	lung:	fetal
50	chr7:39873832-39873882	Hela-S3	cervix:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-9	chr7:39872885-39873392	NONHSAT120235

No data

Variant related genes	Relation type
ENSG00000233225	TF binding region
ENSG00000231198	TF binding region
ENSG00000233225	CpG island
ENSG00000231198	CpG island

Extended variants
information (count: 71 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13438032	chr7:39871991-39871992	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545932137	chr7:39872020-39872021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190808513	chr7:39872084-39872085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181175505	chr7:39872154-39872155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565150416	chr7:39872161-39872162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532538960	chr7:39872164-39872165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552510122	chr7:39872309-39872310	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142871039	chr7:39872358-39872359	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112918732	chr7:39872359-39872360	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185824096	chr7:39872418-39872419	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs76516478	chr7:39872507-39872508	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs546974353	chr7:39872544-39872545	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs372227962	chr7:39872573-39872574	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs151051066	chr7:39872574-39872575	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs566396101	chr7:39872606-39872607	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs112243086	chr7:39872668-39872669	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552274036	chr7:39872731-39872732	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs191239404	chr7:39872809-39872810	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs146677923	chr7:39872813-39872814	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531347771	chr7:39872816-39872817	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs531600411	chr7:39872827-39872828	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs112834604	chr7:39872848-39872849	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375555885	chr7:39872853-39872854	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs548611258	chr7:39872894-39872895	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs568242851	chr7:39872898-39872899	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs374722446	chr7:39872912-39872913	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs534129886	chr7:39872935-39872936	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs182691474	chr7:39872973-39872974	Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs570684219	chr7:39873001-39873002	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs539495196	chr7:39873010-39873011	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs556304332	chr7:39873011-39873012	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs369497153	chr7:39873014-39873015	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs113697757	chr7:39873021-39873022	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs13243994	chr7:39873056-39873057	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs13243997	chr7:39873068-39873069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs576125464	chr7:39873106-39873107	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs373624623	chr7:39873126-39873127	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs369035985	chr7:39873127-39873128	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs535099218	chr7:39873150-39873151	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs187601093	chr7:39873160-39873161	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs575016543	chr7:39873169-39873170	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs540540232	chr7:39873178-39873179	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
43	rs192117400	chr7:39873210-39873211	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs56354939	chr7:39873241-39873242	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs577025086	chr7:39873298-39873299	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs537080772	chr7:39873299-39873300	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs553958958	chr7:39873316-39873317	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs546029215	chr7:39873323-39873324	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs562639816	chr7:39873386-39873387	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs531861165	chr7:39873435-39873436	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39866600-39872400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr7:39866800-39872400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:39872200-39872400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:39872200-39872400	Bivalent Enhancer	NHDF-Ad	bronchial
5	chr7:39872400-39872600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
6	chr7:39872400-39872600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:39872400-39872600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:39872400-39872600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:39872400-39872600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:39872400-39872600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr7:39872400-39872600	Enhancers	Brain Substantia Nigra	brain
12	chr7:39872400-39872600	Bivalent Enhancer	Colon Smooth Muscle	Colon
13	chr7:39872400-39872600	Bivalent Enhancer	Duodenum Mucosa	Duodenum
14	chr7:39872400-39872600	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr7:39872400-39872600	Bivalent Enhancer	Stomach Mucosa	stomach
16	chr7:39872400-39872600	Bivalent/Poised TSS	GM12878-XiMat	blood
17	chr7:39872400-39872800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr7:39872400-39872800	Enhancers	NHDF-Ad	bronchial
19	chr7:39872400-39873000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
20	chr7:39872400-39873000	Bivalent Enhancer	HUVEC	blood vessel
21	chr7:39872400-39873200	Active TSS	Primary hematopoietic stem cells short term culture	blood
22	chr7:39872400-39873200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr7:39872400-39873400	Bivalent/Poised TSS	Fetal Kidney	kidney
24	chr7:39872400-39873400	Active TSS	HMEC	breast
25	chr7:39872400-39873600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:39872400-39873800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr7:39872400-39874200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
28	chr7:39872400-39874400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
29	chr7:39872400-39874400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr7:39872600-39872800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr7:39872600-39872800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
32	chr7:39872600-39873000	Enhancers	Adipose Nuclei	Adipose
33	chr7:39872600-39873200	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:39872600-39873200	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
35	chr7:39872600-39873200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:39872600-39873200	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr7:39872600-39873200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr7:39872600-39873200	Bivalent/Poised TSS	Fetal Intestine Large	intestine
39	chr7:39872600-39873200	Active TSS	Fetal Muscle Leg	muscle
40	chr7:39872600-39873200	Bivalent/Poised TSS	Fetal Stomach	stomach
41	chr7:39872600-39873400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:39872600-39873400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:39872600-39873400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
44	chr7:39872600-39873400	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr7:39872600-39873600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:39872600-39873600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr7:39872600-39873600	Active TSS	Brain Hippocampus Middle	brain
48	chr7:39872600-39873800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:39872600-39874000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:39872600-39874200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell

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