Variant report

Variant	nsv365384
Chromosome Location	chr7:127997292-128001042
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	CEBPB	chr7:127998346-127998657	K562	blood:	n/a	chr7:127998509-127998522 chr7:127998511-127998522
2	CHD2	chr7:128000841-128000842	HepG2	liver:	n/a	n/a
3	CHD2	chr7:128000769-128001074	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr7:127997820-127997970	BE2_C	brain:	n/a	chr7:127997887-127997900 chr7:127997880-127997901 chr7:127997885-127997903
5	CTCF	chr7:127997420-127997570	SK-N-SH_RA	brain:	n/a	n/a
6	CTCF	chr7:127997740-127997890	SK-N-SH_RA	brain:	n/a	n/a
7	CTCF	chr7:127997760-127997910	SK-N-SH_RA	brain:	n/a	chr7:127997887-127997900 chr7:127997880-127997901 chr7:127997885-127997903
8	EP300	chr7:128000483-128001084	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr7:128000634-128001096	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr7:127994619-127999337	SK-N-SH	brain:	n/a	chr7:127996599-127996613 chr7:127998510-127998524
11	EP300	chr7:127999704-128005454	SK-N-SH	brain:	n/a	chr7:128001515-128001531 chr7:128001869-128001885 chr7:128001522-128001531 chr7:128003957-128003966 chr7:128001589-128001605 chr7:128001670-128001679 chr7:128003305-128003319 chr7:128001721-128001737 chr7:128003956-128003970 chr7:128003346-128003362 chr7:128001590-128001606 chr7:128003823-128003832
12	EP300	chr7:127997169-127998019	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr7:127997207-127997768	SK-N-SH_RA	brain:	n/a	n/a
14	GATA2	chr7:127996416-127997799	SH-SY5Y	brain:	n/a	n/a
15	GATA3	chr7:127996431-127997837	SK-N-SH	brain:	n/a	n/a
16	GATA3	chr7:127996407-127997837	SK-N-SH	brain:	n/a	n/a
17	MAFK	chr7:127998598-127998745	HepG2	liver:	n/a	n/a
18	MAX	chr7:128000724-128001564	H1-hESC	embryonic stem cell:	n/a	chr7:128001115-128001125
19	MAX	chr7:128000419-128002482	NB4	blood:	n/a	chr7:128001115-128001125 chr7:128002065-128002075
20	MAZ	chr7:128000968-128001042	HepG2	liver:	n/a	n/a
21	MXI1	chr7:127999698-128004914	SK-N-SH	brain:	n/a	n/a
22	MYC	chr7:127998256-127999001	NB4	blood:	n/a	chr7:127998981-127998997
23	MYC	chr7:128000401-128002498	NB4	blood:	n/a	chr7:128001115-128001125 chr7:128002065-128002075
24	PBX3	chr7:127996578-127997786	SK-N-SH	brain:	n/a	n/a
25	PBX3	chr7:127996469-127997809	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr7:128000494-128002408	NB4	blood:	n/a	n/a
27	POLR2A	chr7:128000846-128001480	SK-N-SH	brain:	n/a	n/a
28	POLR2A	chr7:128000242-128001516	HL-60	blood:	n/a	n/a
29	POLR2A	chr7:128000741-128002458	H1-neurons	neurons:	n/a	n/a
30	POLR2A	chr7:127997345-127997804	SK-N-SH	brain:	n/a	n/a
31	POLR2A	chr7:128000705-128002491	H1-neurons	neurons:	n/a	n/a
32	POLR2A	chr7:128000562-128002554	HL-60	blood:	n/a	n/a
33	POLR2A	chr7:127997172-127997802	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr7:128000389-128001473	SK-N-MC	brain:	n/a	n/a
35	POLR2A	chr7:128000283-128001620	SK-N-MC	brain:	n/a	n/a
36	RAD21	chr7:127997278-127997710	SK-N-SH_RA	brain:	n/a	n/a
37	RAD21	chr7:127997214-127997751	SK-N-SH_RA	brain:	n/a	n/a
38	RAD21	chr7:128000455-128001014	SK-N-SH_RA	brain:	n/a	chr7:128000599-128000609 chr7:128000599-128000611
39	RCOR1	chr7:127998385-127998604	K562	blood:	n/a	n/a
40	REST	chr7:127997465-127997744	SK-N-SH	brain:	n/a	chr7:127997594-127997607 chr7:127997512-127997519
41	REST	chr7:127997471-127997723	H1-hESC	embryonic stem cell:	n/a	chr7:127997594-127997607 chr7:127997512-127997519
42	REST	chr7:127997387-127997750	PFSK-1	brain:	n/a	chr7:127997594-127997607 chr7:127997512-127997519
43	REST	chr7:128000378-128000702	SK-N-SH	brain:	n/a	n/a
44	REST	chr7:128000595-128002632	H1-neurons	neurons:	n/a	chr7:128001926-128001933 chr7:128001630-128001643 chr7:128001593-128001606 chr7:128001515-128001525
45	REST	chr7:127997252-127997944	SK-N-SH	brain:	n/a	chr7:127997594-127997607 chr7:127997512-127997519
46	REST	chr7:127997487-127997744	PANC-1	pancreas:	n/a	chr7:127997594-127997607 chr7:127997512-127997519
47	REST	chr7:127997382-127997710	PFSK-1	brain:	n/a	chr7:127997594-127997607 chr7:127997512-127997519
48	REST	chr7:128000718-128001116	SK-N-SH	brain:	n/a	n/a
49	SIN3A	chr7:128000732-128001705	H1-hESC	embryonic stem cell:	n/a	chr7:128001434-128001445 chr7:128001593-128001606 chr7:128001583-128001596
50	TAF1	chr7:128000628-128002274	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:127997529-127997579	HepG2	liver:	n/a
2	chr7:128000861-128000911	AG09319	gingival:	n/a
3	chr7:127997529-127997579	HepG2	liver:	n/a
4	chr7:128000861-128000911	AG09319	gingival:	n/a
5	chr7:128000780-128000830	HRCEpiC	kidney:	n/a
6	chr7:127997529-127997579	CMK	blood:	n/a
7	chr7:127997529-127997579	AoSMC	blood vessel:	n/a
8	chr7:128000780-128000830	NB4	blood:	n/a
9	chr7:128000861-128000911	PANC-1	pancreas:	n/a
10	chr7:128000780-128000830	SK-N-SH_RA	brain:	n/a
11	chr7:128000780-128000830	HIPEpiC	eye:	n/a
12	chr7:127997529-127997579	NT2-D1	testis:	n/a
13	chr7:128000861-128000911	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:127997529-127997579	NB4	blood:	n/a
15	chr7:128000780-128000830	BJ	skin:	n/a
16	chr7:128000780-128000830	ProgFib	skin:	n/a
17	chr7:127997529-127997579	HNPCEpiC	eye:	n/a
18	chr7:128000861-128000911	GM12892	blood:	n/a
19	chr7:128000780-128000830	HRE	kidney:	n/a
20	chr7:128000780-128000830	ECC-1	luminal epithelium:	n/a
21	chr7:128000861-128000911	HAEpiC	amniotic membrane:	n/a
22	chr7:128000780-128000830	HNPCEpiC	eye:	n/a
23	chr7:128000861-128000911	SKMC	muscle:	n/a
24	chr7:128000780-128000830	HUVEC	blood vessel:	n/a
25	chr7:127997529-127997579	NHDF-neo	bronchial:	n/a
26	chr7:127997529-127997579	NH-A	brain:	n/a
27	chr7:128000861-128000911	GM12878	blood:	n/a
28	chr7:127997529-127997579	GM06990	blood:	n/a
29	chr7:127997529-127997579	SAEC	small airway:	n/a
30	chr7:127997529-127997579	HEEpiC	esophagus:	n/a
31	chr7:128000780-128000830	NT2-D1	testis:	n/a
32	chr7:127997529-127997579	ProgFib	skin:	n/a
33	chr7:128000780-128000830	HCF	heart:	n/a
34	chr7:128000780-128000830	Jurkat	blood:	n/a
35	chr7:128000861-128000911	T-47D	breast:	n/a
36	chr7:127997529-127997579	HCPEpiC	choroid plexus:	n/a
37	chr7:127997529-127997579	PFSK-1	brain:	n/a
38	chr7:128000861-128000911	IMR90	lung:	fetal
39	chr7:127997529-127997579	H1-hESC	embryonic stem cell:	embryo
40	chr7:127997529-127997579	SK-N-SH	brain:	n/a
41	chr7:128000861-128000911	PFSK-1	brain:	n/a
42	chr7:128000861-128000911	ovcar-3	ovarian:	n/a
43	chr7:128000780-128000830	AG10803	skin:	n/a
44	chr7:128000861-128000911	NB4	blood:	n/a
45	chr7:127997529-127997579	Jurkat	blood:	n/a
46	chr7:128000780-128000830	HMEC	breast:	n/a
47	chr7:128000861-128000911	GM06990	blood:	n/a
48	chr7:127997529-127997579	ECC-1	luminal epithelium:	n/a
49	chr7:128000861-128000911	Jurkat	blood:	n/a
50	chr7:128000780-128000830	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:127996352..127999445-chr7:128029289..128030923,3	K562	blood:
2	chr7:127996426..127998366-chr7:128029110..128031908,2	MCF-7	breast:
3	chr7:127993467..127995133-chr7:127996193..127999094,2	K562	blood:
4	chr7:127994580..127997390-chr7:128003356..128005178,2	MCF-7	breast:
5	chr7:127988724..127990769-chr7:127995960..127998093,2	MCF-7	breast:
6	chr7:127987637..127990032-chr7:127996587..127999428,2	MCF-7	breast:
7	chr7:127984024..127986561-chr7:127997384..127999577,3	K562	blood:
8	chr7:127981245..127984643-chr7:127995336..127998273,3	MCF-7	breast:
9	chr7:127997986..128000354-chr7:128001685..128004213,3	K562	blood:

Variant related genes	Relation type
PRRT4	TF binding region
PRRT4	CpG island
ENSG00000224940	chromatin interactions
ENSG00000238750	chromatin interactions
ENSG00000106344	chromatin interactions

Extended variants
information (count: 146 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:146 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7786215	chr7:127997292-127997293	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs62481083	chr7:127997294-127997295	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs62481084	chr7:127997296-127997297	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs62481085	chr7:127997298-127997299	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543961312	chr7:127997300-127997301	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142887120	chr7:127997302-127997303	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs151316371	chr7:127997304-127997305	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs142048588	chr7:127997306-127997307	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs60699919	chr7:127997319-127997320	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185487714	chr7:127997326-127997327	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs373602426	chr7:127997348-127997349	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35901471	chr7:127997401-127997402	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs530034603	chr7:127997451-127997452	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs541826479	chr7:127997464-127997465	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs561197044	chr7:127997498-127997499	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs561003991	chr7:127997534-127997535	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531526191	chr7:127997543-127997544	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549922178	chr7:127997544-127997545	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571336056	chr7:127997545-127997546	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs149820062	chr7:127997549-127997550	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs359641	chr7:127997570-127997571	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190013369	chr7:127997645-127997646	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536211813	chr7:127997650-127997651	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554281701	chr7:127997661-127997662	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs570300871	chr7:127997685-127997686	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs537321183	chr7:127997703-127997704	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559236038	chr7:127997725-127997726	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs192054963	chr7:127997730-127997731	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147936669	chr7:127997739-127997740	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140157011	chr7:127997759-127997760	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73230664	chr7:127997762-127997763	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374468594	chr7:127997769-127997770	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs530559907	chr7:127997818-127997819	Genic enhancers Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377515450	chr7:127997864-127997865	Genic enhancers Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs118173665	chr7:127997913-127997914	Genic enhancers Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs530964421	chr7:127997932-127997933	Genic enhancers Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs184283263	chr7:127997964-127997965	Genic enhancers Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188623709	chr7:127997977-127997978	Genic enhancers Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs538172777	chr7:127998008-127998009	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs181048676	chr7:127998016-127998017	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs552193860	chr7:127998024-127998025	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs565744386	chr7:127998052-127998053	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs147756967	chr7:127998100-127998101	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550408926	chr7:127998126-127998127	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs548292326	chr7:127998131-127998132	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs569129951	chr7:127998187-127998188	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs183772134	chr7:127998196-127998197	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs558983513	chr7:127998214-127998215	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs149135237	chr7:127998237-127998238	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs545490324	chr7:127998294-127998295	Genic enhancers Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127992800-128000600	Weak transcription	Right Atrium	heart
2	chr7:127995800-128000200	Weak transcription	Ovary	ovary
3	chr7:127996000-127997400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr7:127996400-127997400	Enhancers	HSMM	muscle
5	chr7:127996400-127997600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:127996400-127998000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
7	chr7:127996400-127998000	Enhancers	Fetal Heart	heart
8	chr7:127996400-127998400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr7:127996600-127998200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr7:127996800-127997800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:127996800-127997800	Bivalent Enhancer	Fetal Stomach	stomach
12	chr7:127997000-127997600	Enhancers	Right Ventricle	heart
13	chr7:127997000-127997800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:127997000-127997800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
15	chr7:127997000-128000400	Enhancers	Adipose Nuclei	Adipose
16	chr7:127997000-128001000	Weak transcription	HSMMtube	muscle
17	chr7:127997200-127998000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:127997200-128001000	Weak transcription	Left Ventricle	heart
19	chr7:127997400-127997800	Weak transcription	Spleen	Spleen
20	chr7:127997400-127999800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:127997400-128000400	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr7:127997400-128000400	Weak transcription	HSMM	muscle
23	chr7:127997600-127997800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
24	chr7:127997600-127997800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr7:127997600-127997800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:127997600-127997800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
27	chr7:127997600-127997800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr7:127997600-127998000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr7:127997600-128000400	Weak transcription	Right Ventricle	heart
30	chr7:127997600-128000400	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr7:127997600-128000600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr7:127997600-128000800	Enhancers	Primary B cells from cord blood	blood
33	chr7:127997800-127998400	Enhancers	Spleen	Spleen
34	chr7:127997800-127999000	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:127997800-127999000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr7:127998000-127998400	Enhancers	Primary hematopoietic stem cells	blood
37	chr7:127998000-128000800	Weak transcription	Fetal Heart	heart
38	chr7:127998200-128001000	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr7:127998400-127998600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr7:127998400-127999400	Weak transcription	Spleen	Spleen
41	chr7:127998400-127999800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:127998400-128000000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:127998400-128000400	Weak transcription	Primary hematopoietic stem cells	blood
44	chr7:127999000-128000800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr7:127999400-127999600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr7:127999400-127999600	Enhancers	Spleen	Spleen
47	chr7:127999400-128000400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:127999600-128000000	Weak transcription	Spleen	Spleen
49	chr7:127999800-128000200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:127999800-128000800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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