Variant report

Variant	esv3430564
Chromosome Location	chr7:153747469-153751467
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	BATF	chr7:153751061-153751258	GM12878	blood:	n/a	n/a
2	CTCF	chr7:153748458-153748743	GM12891	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
3	CTCF	chr7:153748720-153748870	SK-N-SH_RA	brain:	n/a	n/a
4	CTCF	chr7:153748494-153748709	Kidney_OC	kidney:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
5	CTCF	chr7:153750640-153750790	BE2_C	brain:	n/a	n/a
6	CTCF	chr7:153748452-153748773	MCF-7	breast:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
7	CTCF	chr7:153748474-153748772	LNCaP	prostate:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
8	CTCF	chr7:153748454-153748771	MCF-7	breast:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
9	CTCF	chr7:153748395-153748921	K562	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
10	CTCF	chr7:153749380-153749530	BE2_C	brain:	n/a	chr7:153749496-153749517 chr7:153749494-153749512
11	CTCF	chr7:153748533-153748666	Lung_OC	lung:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
12	CTCF	chr7:153747971-153747988	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr7:153748504-153748727	GM12878	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
14	CTCF	chr7:153749448-153749552	H1-hESC	embryonic stem cell:	n/a	chr7:153749496-153749517 chr7:153749494-153749512
15	CTCF	chr7:153750640-153750790	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr7:153748462-153748766	MCF-7	breast:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
17	CTCF	chr7:153749467-153749556	Medullo	brain:	n/a	chr7:153749496-153749517 chr7:153749494-153749512
18	CTCF	chr7:153748471-153748737	Fibrobl	skin:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
19	CTCF	chr7:153748481-153748711	GM10248	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
20	CTCF	chr7:153748464-153748735	NHEK	skin:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
21	CTCF	chr7:153748486-153748492	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr7:153748449-153748739	H1-hESC	embryonic stem cell:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
23	CTCF	chr7:153748512-153748767	LNCaP	prostate:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
24	CTCF	chr7:153748482-153748731	K562	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
25	CTCF	chr7:153748470-153748737	MCF-7	breast:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
26	CTCF	chr7:153748467-153748705	A549	lung:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
27	CTCF	chr7:153748354-153748751	A549	lung:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
28	CTCF	chr7:153748455-153748733	Gliobla	brain:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
29	CTCF	chr7:153748568-153748571	GM13976	blood:	n/a	n/a
30	CTCF	chr7:153748488-153748692	HUVEC	blood vessel:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
31	CTCF	chr7:153748502-153748691	Hela-S3	cervix:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
32	CTCF	chr7:153748490-153748723	GM19240	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
33	CTCF	chr7:153748491-153748730	HepG2	liver:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
34	CTCF	chr7:153748473-153748749	A549	lung:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
35	CTCF	chr7:153748435-153748733	A549	lung:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
36	CTCF	chr7:153748476-153748718	ProgFib	skin:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
37	CTCF	chr7:153748493-153748743	GM19238	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
38	CTCF	chr7:153749995-153750006	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr7:153748477-153748697	GM12892	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
40	CTCF	chr7:153748497-153748710	GM13977	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
41	CTCF	chr7:153748470-153748752	Pancreas_OC	pancreas:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
42	CTCF	chr7:153748464-153748757	MCF-7	breast:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
43	CTCF	chr7:153748396-153748804	K562	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
44	CTCF	chr7:153748392-153748812	K562	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
45	CTCF	chr7:153748504-153748712	Spleen_OC	spleen:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
46	CTCF	chr7:153748458-153748762	A549	lung:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
47	CTCF	chr7:153750582-153750626	Gliobla	brain:	n/a	n/a
48	CTCF	chr7:153748483-153748720	GM19239	blood:	n/a	chr7:153748578-153748591 chr7:153748618-153748631
49	CTCF	chr7:153749360-153749510	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:153748597-153748637	GM13976	blood:	n/a	chr7:153748618-153748631

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153749738-153749788	SK-N-MC	brain:	n/a
2	chr7:153749738-153749788	SK-N-MC	brain:	n/a
3	chr7:153748818-153748868	MCF10A-Er-Src	breast:	n/a
4	chr7:153748370-153748420	ProgFib	skin:	n/a
5	chr7:153749759-153749809	HCT-116	colon:	n/a
6	chr7:153749756-153749806	LNCaP	prostate:	n/a
7	chr7:153750421-153750471	GM12878	blood:	n/a
8	chr7:153751298-153751348	ECC-1	luminal epithelium:	n/a
9	chr7:153748818-153748868	AG10803	skin:	n/a
10	chr7:153748818-153748868	HNPCEpiC	eye:	n/a
11	chr7:153749738-153749788	U87	brain:	n/a
12	chr7:153748370-153748420	HEEpiC	esophagus:	n/a
13	chr7:153747525-153747575	HAEpiC	amniotic membrane:	n/a
14	chr7:153749756-153749806	AoSMC	blood vessel:	n/a
15	chr7:153747525-153747575	HCPEpiC	choroid plexus:	n/a
16	chr7:153749736-153749786	K562	blood:	n/a
17	chr7:153749964-153750014	NH-A	brain:	n/a
18	chr7:153749736-153749786	HCF	heart:	n/a
19	chr7:153751298-153751348	RPTEC	kidney:	n/a
20	chr7:153750421-153750471	NH-A	brain:	n/a
21	chr7:153751298-153751348	PrEC	prostate:	n/a
22	chr7:153749206-153749256	NHDF-neo	bronchial:	n/a
23	chr7:153748370-153748420	K562	blood:	n/a
24	chr7:153748818-153748868	ovcar-3	ovarian:	n/a
25	chr7:153749736-153749786	Jurkat	blood:	n/a
26	chr7:153748370-153748420	AoSMC	blood vessel:	n/a
27	chr7:153751298-153751348	HCF	heart:	n/a
28	chr7:153749206-153749256	AG04449	skin:	fetal
29	chr7:153749964-153750014	GM19239	blood:	n/a
30	chr7:153751298-153751348	AG09309	skin:	n/a
31	chr7:153749736-153749786	PANC-1	pancreas:	n/a
32	chr7:153748818-153748868	AG04449	skin:	fetal
33	chr7:153749964-153750014	GM12878	blood:	n/a
34	chr7:153747525-153747575	HCF	heart:	n/a
35	chr7:153749736-153749786	NHBE	bronchial:	n/a
36	chr7:153749206-153749256	ProgFib	skin:	n/a
37	chr7:153751298-153751348	ProgFib	skin:	n/a
38	chr7:153747525-153747575	NHDF-neo	bronchial:	n/a
39	chr7:153749736-153749786	PFSK-1	brain:	n/a
40	chr7:153749759-153749809	HRCEpiC	kidney:	n/a
41	chr7:153749756-153749806	SK-N-SH	brain:	n/a
42	chr7:153749736-153749786	HEEpiC	esophagus:	n/a
43	chr7:153748370-153748420	AG10803	skin:	n/a
44	chr7:153747525-153747575	GM12891	blood:	n/a
45	chr7:153747525-153747575	HNPCEpiC	eye:	n/a
46	chr7:153747525-153747575	SKMC	muscle:	n/a
47	chr7:153749756-153749806	PANC-1	pancreas:	n/a
48	chr7:153748370-153748420	HCT-116	colon:	n/a
49	chr7:153749206-153749256	HNPCEpiC	eye:	n/a
50	chr7:153749738-153749788	SKMC	muscle:	n/a

Variant related genes	Relation type
DPP6	TF binding region
DPP6	CpG island

Extended variants
information (count: 183 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:183 , 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	rs566943564	chr7:153747484-153747485	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs182782172	chr7:153747505-153747506	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs2628696	chr7:153747526-153747527	Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs549471325	chr7:153747561-153747562	Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs374428258	chr7:153747587-153747588	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs571484731	chr7:153747595-153747596	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs571702573	chr7:153747596-153747597	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs28508192	chr7:153747833-153747834	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs566346695	chr7:153747846-153747847	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs536975099	chr7:153747848-153747849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs538424577	chr7:153747862-153747863	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs576125798	chr7:153747878-153747879	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140649523	chr7:153747879-153747880	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs554975144	chr7:153747908-153747909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs58597627	chr7:153747919-153747920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs543895803	chr7:153747920-153747921	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs184517511	chr7:153747950-153747951	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs187855706	chr7:153748028-153748029	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs545180861	chr7:153748051-153748052	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs1860506	chr7:153748156-153748157	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs2533737	chr7:153748188-153748189	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2533736	chr7:153748194-153748195	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs1860505	chr7:153748201-153748202	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs542526629	chr7:153748238-153748239	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs201357494	chr7:153748264-153748265	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs560505110	chr7:153748290-153748291	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs555292964	chr7:153748292-153748293	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs531207405	chr7:153748295-153748296	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs549557664	chr7:153748300-153748301	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs571310528	chr7:153748314-153748315	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs57132253	chr7:153748330-153748331	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2533735	chr7:153748382-153748383	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs184219635	chr7:153748404-153748405	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs377371714	chr7:153748434-153748435	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs555312276	chr7:153748466-153748467	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191240662	chr7:153748467-153748468	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs537441863	chr7:153748476-153748477	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62485597	chr7:153748482-153748483	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs62485598	chr7:153748492-153748493	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs374900042	chr7:153748497-153748498	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs577254558	chr7:153748502-153748503	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs545585103	chr7:153748506-153748507	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs139411342	chr7:153748515-153748516	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs368539833	chr7:153748526-153748527	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs527334726	chr7:153748533-153748534	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs59213906	chr7:153748535-153748536	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs542463352	chr7:153748540-153748541	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs542741064	chr7:153748553-153748554	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs370281296	chr7:153748561-153748562	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs575971854	chr7:153748567-153748568	Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153747400-153747600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
2	chr7:153748000-153748200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:153748000-153748200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr7:153748000-153748200	Enhancers	Stomach Smooth Muscle	stomach
5	chr7:153748000-153748400	Enhancers	Rectal Smooth Muscle	rectum
6	chr7:153748000-153748600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
7	chr7:153748000-153748800	Active TSS	H1 Cell Line	embryonic stem cell
8	chr7:153748000-153748800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:153748000-153749600	Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr7:153748000-153749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:153748000-153750800	Active TSS	Brain Anterior Caudate	brain
12	chr7:153748000-153751400	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr7:153748200-153748400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
14	chr7:153748200-153748400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
15	chr7:153748200-153748400	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr7:153748200-153748400	Bivalent Enhancer	Lung	lung
17	chr7:153748200-153748400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr7:153748200-153748600	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr7:153748200-153748800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:153748200-153749000	Enhancers	Adipose Nuclei	Adipose
21	chr7:153748200-153749000	Active TSS	Brain Angular Gyrus	brain
22	chr7:153748200-153749000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
23	chr7:153748200-153749600	Active TSS	Brain Germinal Matrix	brain
24	chr7:153748200-153749800	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr7:153748200-153750000	Active TSS	Stomach Smooth Muscle	stomach
26	chr7:153748200-153750400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr7:153748200-153750400	Active TSS	Brain Hippocampus Middle	brain
28	chr7:153748200-153750600	Active TSS	iPS-15b Cell Line	embryonic stem cell
29	chr7:153748200-153750800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr7:153748200-153751600	Active TSS	Fetal Brain Female	brain
31	chr7:153748400-153748800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
32	chr7:153748400-153749000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr7:153748400-153750400	Active TSS	Brain Cingulate Gyrus	brain
34	chr7:153748400-153750600	Active TSS	H9 Cell Line	embryonic stem cell
35	chr7:153748400-153750800	Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr7:153748400-153750800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr7:153748600-153749400	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr7:153748600-153750800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
39	chr7:153748800-153749000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr7:153748800-153749000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
41	chr7:153748800-153749000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
42	chr7:153748800-153749000	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
43	chr7:153748800-153749400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:153748800-153749600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:153748800-153750000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr7:153748800-153750400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:153748800-153750400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:153748800-153750400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:153748800-153750400	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr7:153748800-153750800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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