Variant report

Variant	nsv538690
Chromosome Location	chr7:4078345-4166552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:422)
CpG islands
(count:1588)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:4080212-4080618	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:4080072-4080609	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:4079771-4080377	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr7:4143342-4143771	K562	blood:	n/a	n/a
5	CEBPB	chr7:4093841-4094161	K562	blood:	n/a	chr7:4093990-4094001
6	CEBPB	chr7:4093829-4094161	Hela-S3	cervix:	n/a	chr7:4093990-4094001
7	CEBPB	chr7:4143283-4143797	A549	lung:	n/a	chr7:4143746-4143757
8	CEBPB	chr7:4093830-4094161	IMR90	lung:	n/a	chr7:4093990-4094001
9	CEBPB	chr7:4143145-4143844	MCF-7	breast:	n/a	chr7:4143746-4143757
10	CEBPB	chr7:4093806-4094264	MCF-7	breast:	n/a	chr7:4093990-4094001
11	CEBPB	chr7:4133313-4133359	A549	lung:	n/a	n/a
12	CEBPB	chr7:4143302-4143760	H1-hESC	embryonic stem cell:	n/a	chr7:4143746-4143757
13	CEBPB	chr7:4143335-4143889	K562	blood:	n/a	chr7:4143746-4143757
14	CEBPB	chr7:4093839-4094204	MCF-7	breast:	n/a	chr7:4093990-4094001
15	CEBPB	chr7:4078386-4078426	HepG2	liver:	n/a	n/a
16	CEBPB	chr7:4093847-4094117	A549	lung:	n/a	chr7:4093990-4094001
17	CEBPB	chr7:4133326-4133404	K562	blood:	n/a	n/a
18	CEBPB	chr7:4143725-4143868	HepG2	liver:	n/a	chr7:4143746-4143757
19	CEBPB	chr7:4093811-4094173	HepG2	liver:	n/a	chr7:4093990-4094001
20	CEBPB	chr7:4079734-4080061	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:4093892-4094040	HepG2	liver:	n/a	chr7:4093990-4094001
22	CEBPB	chr7:4093833-4094171	A549	lung:	n/a	chr7:4093990-4094001
23	CEBPB	chr7:4164281-4164504	HepG2	liver:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
24	CEBPB	chr7:4164261-4164462	A549	lung:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
25	CEBPB	chr7:4098994-4099005	IMR90	lung:	n/a	n/a
26	CEBPZ	chr7:4098999-4099105	HepG2	liver:	n/a	n/a
27	CHD1	chr7:4080537-4080654	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr7:4143451-4143520	K562	blood:	n/a	n/a
29	CHD2	chr7:4079532-4080515	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr7:4114732-4114984	A549	lung:	n/a	n/a
31	CTCF	chr7:4143140-4143290	HRPEpiC	eye:	n/a	chr7:4143161-4143179
32	CTCF	chr7:4114720-4114870	WERI-Rb-1	eye:	n/a	chr7:4114833-4114842
33	CTCF	chr7:4142020-4142170	HepG2	liver:	n/a	n/a
34	CTCF	chr7:4143120-4143270	Caco-2	colon:	n/a	chr7:4143161-4143179
35	CTCF	chr7:4143060-4143210	HUVEC	blood vessel:	n/a	chr7:4143161-4143179
36	CTCF	chr7:4143160-4143310	HRE	kidney:	n/a	chr7:4143161-4143179
37	CTCF	chr7:4143120-4143270	NB4	blood:	n/a	chr7:4143161-4143179
38	CTCF	chr7:4114640-4114790	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr7:4143160-4143310	HEK293	kidney:	n/a	chr7:4143161-4143179
40	CTCF	chr7:4143320-4143470	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr7:4142480-4142630	HAc	cerebellar:	n/a	n/a
42	CTCF	chr7:4143093-4143279	A549	lung:	n/a	chr7:4143161-4143179
43	CTCF	chr7:4143060-4143210	HA-sp	spinal cord:	n/a	chr7:4143161-4143179
44	CTCF	chr7:4142880-4143030	HAc	cerebellar:	n/a	n/a
45	CTCF	chr7:4142962-4143587	A549	lung:	n/a	chr7:4143161-4143179
46	CTCF	chr7:4114723-4114853	MCF-7	breast:	n/a	chr7:4114833-4114842
47	CTCF	chr7:4143080-4143230	HCT-116	colon:	n/a	chr7:4143161-4143179
48	CTCF	chr7:4114756-4114809	MCF-7	breast:	n/a	n/a
49	CTCF	chr7:4143180-4143330	RPTEC	kidney:	n/a	n/a
50	CTCF	chr7:4143000-4143150	NHEK	skin:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4157691-4157741	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:4147330-4147380	AG10803	skin:	n/a
3	chr7:4157691-4157741	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:4147330-4147380	AG10803	skin:	n/a
5	chr7:4118868-4118918	PANC-1	pancreas:	n/a
6	chr7:4113480-4113530	BE2_C	brain:	n/a
7	chr7:4147330-4147380	HAEpiC	amniotic membrane:	n/a
8	chr7:4150753-4150803	SK-N-SH	brain:	n/a
9	chr7:4157691-4157741	HCF	heart:	n/a
10	chr7:4085305-4085355	K562	blood:	n/a
11	chr7:4153868-4153918	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:4153732-4153782	MCF10A-Er-Src	breast:	n/a
13	chr7:4157691-4157741	AG10803	skin:	n/a
14	chr7:4133359-4133409	SKMC	muscle:	n/a
15	chr7:4118685-4118735	GM12878	blood:	n/a
16	chr7:4147274-4147324	NHDF-neo	bronchial:	n/a
17	chr7:4153767-4153817	GM06990	blood:	n/a
18	chr7:4153732-4153782	GM06990	blood:	n/a
19	chr7:4133359-4133409	HCT-116	colon:	n/a
20	chr7:4147274-4147324	HEEpiC	esophagus:	n/a
21	chr7:4146971-4147021	T-47D	breast:	n/a
22	chr7:4153919-4153969	AG04449	skin:	fetal
23	chr7:4150753-4150803	AG09319	gingival:	n/a
24	chr7:4118583-4118633	BE2_C	brain:	n/a
25	chr7:4153919-4153969	CMK	blood:	n/a
26	chr7:4118583-4118633	LNCaP	prostate:	n/a
27	chr7:4118609-4118659	HRPEpiC	eye:	n/a
28	chr7:4147432-4147482	GM12892	blood:	n/a
29	chr7:4133359-4133409	AG04449	skin:	fetal
30	chr7:4153732-4153782	IMR90	lung:	fetal
31	chr7:4085257-4085307	GM12878	blood:	n/a
32	chr7:4085305-4085355	NHBE	bronchial:	n/a
33	chr7:4153919-4153969	AG09309	skin:	n/a
34	chr7:4147432-4147482	HAEpiC	amniotic membrane:	n/a
35	chr7:4146971-4147021	HNPCEpiC	eye:	n/a
36	chr7:4118583-4118633	AG04450	lung:	fetal
37	chr7:4147274-4147324	HEK293	kidney:	embryo
38	chr7:4146971-4147021	AoSMC	blood vessel:	n/a
39	chr7:4153732-4153782	HUVEC	blood vessel:	n/a
40	chr7:4147432-4147482	HNPCEpiC	eye:	n/a
41	chr7:4153868-4153918	SKMC	muscle:	n/a
42	chr7:4147330-4147380	AG09309	skin:	n/a
43	chr7:4153707-4153757	GM12891	blood:	n/a
44	chr7:4150753-4150803	GM06990	blood:	n/a
45	chr7:4118609-4118659	SAEC	small airway:	n/a
46	chr7:4085241-4085291	ECC-1	luminal epithelium:	n/a
47	chr7:4147330-4147380	AoSMC	blood vessel:	n/a
48	chr7:4147432-4147482	Jurkat	blood:	n/a
49	chr7:4146291-4146341	LNCaP	prostate:	n/a
50	chr7:4147330-4147380	GM19239	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:4126299..4129076-chr7:4130764..4133447,2	K562	blood:
2	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
3	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:
4	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
5	chr7:4133522..4135936-chr7:4136765..4138658,2	K562	blood:
6	chr7:4088154..4090375-chr7:4090451..4092964,2	MCF-7	breast:
7	chr7:4082285..4084220-chr7:4087738..4090486,2	K562	blood:
8	chr7:4091304..4093218-chr7:4095226..4096867,2	K562	blood:
9	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:
10	chr7:4088154..4090375-chr7:4090451..4092964,2	MCF-7	breast:
11	chr7:4091304..4093218-chr7:4095226..4096867,2	K562	blood:
12	chr7:4143002..4143685-chr7:4518859..4519662,3	MCF-7	breast:
13	chr7:4126299..4129076-chr7:4130764..4133447,2	K562	blood:
14	chr7:4082285..4084220-chr7:4087738..4090486,2	K562	blood:
15	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
16	chr7:4130773..4135650-chr7:4142053..4144303,4	MCF-7	breast:
17	chr7:4149016..4150999-chr7:4154652..4156380,2	K562	blood:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island

Extended variants
information (count: 4975 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:4975 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576063347	chr7:4078380-4078381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545081896	chr7:4078391-4078392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181258842	chr7:4078401-4078402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138750049	chr7:4078431-4078432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7805933	chr7:4078440-4078441	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs560784596	chr7:4078490-4078491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564500770	chr7:4078503-4078504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529563676	chr7:4078513-4078514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549112415	chr7:4078540-4078541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569192071	chr7:4078613-4078614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7806117	chr7:4078618-4078619	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs79930248	chr7:4078621-4078622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571142920	chr7:4078637-4078638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533753011	chr7:4078677-4078678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186516914	chr7:4078678-4078679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567450020	chr7:4078700-4078701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536503981	chr7:4078790-4078791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555923142	chr7:4078791-4078792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7807487	chr7:4078798-4078799	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558671387	chr7:4078884-4078885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572138952	chr7:4078899-4078900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191020644	chr7:4078910-4078911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs137937564	chr7:4078934-4078935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558626575	chr7:4078935-4078936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11450665	chr7:4078944-4078945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10254902	chr7:4078946-4078947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146249183	chr7:4078954-4078955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10236620	chr7:4078988-4078989	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs562770118	chr7:4078992-4078993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531001650	chr7:4079003-4079004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142414484	chr7:4079048-4079049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551326215	chr7:4079092-4079093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10265219	chr7:4079099-4079100	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs10255034	chr7:4079114-4079115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547196304	chr7:4079120-4079121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139254667	chr7:4079143-4079144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10255116	chr7:4079148-4079149	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs182057273	chr7:4079174-4079175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs569587059	chr7:4079244-4079245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78618516	chr7:4079256-4079257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558559950	chr7:4079273-4079274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186688545	chr7:4079299-4079300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572175726	chr7:4079362-4079363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541088018	chr7:4079363-4079364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6462545	chr7:4079412-4079413	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs149378924	chr7:4079423-4079424	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs78923606	chr7:4079437-4079438	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs80084741	chr7:4079438-4079439	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs6462546	chr7:4079451-4079452	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs576448872	chr7:4079454-4079455	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:674 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4059000-4091200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:4061400-4080800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:4066800-4082000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:4066800-4087200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:4066800-4091200	Weak transcription	Pancreas	Pancrea
6	chr7:4073800-4079200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr7:4074000-4078400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:4074000-4078400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:4074000-4079200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:4074000-4079600	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:4074200-4079200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:4077800-4087800	Weak transcription	Spleen	Spleen
13	chr7:4078000-4091200	Weak transcription	Aorta	Aorta
14	chr7:4078400-4078600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:4078400-4078600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr7:4078400-4078800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr7:4078400-4078800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr7:4078400-4081200	Weak transcription	Fetal Muscle Leg	muscle
19	chr7:4078600-4079000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:4078600-4079600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:4078800-4079000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:4078800-4079200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:4079000-4079600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:4079000-4080000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr7:4079200-4079800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr7:4079200-4080000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr7:4079200-4080200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:4079200-4080200	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:4079400-4079600	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr7:4079600-4079800	Enhancers	H9 Cell Line	embryonic stem cell
31	chr7:4079600-4080000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:4079600-4080200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
33	chr7:4079600-4080800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr7:4079600-4081400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:4079600-4083800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:4079800-4080200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
37	chr7:4079800-4080200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr7:4079800-4080200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr7:4079800-4080400	Active TSS	H9 Cell Line	embryonic stem cell
40	chr7:4079800-4080400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:4080000-4080200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
42	chr7:4080000-4080400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr7:4080200-4080600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr7:4080200-4081200	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr7:4080200-4081600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr7:4080200-4082000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:4080200-4083800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr7:4080200-4083800	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr7:4080200-4083800	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr7:4080400-4080600	Flanking Active TSS	H9 Cell Line	embryonic stem cell

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