Variant report

Variant	nsv538942
Chromosome Location	chr7:71552185-71736068
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:510)
CpG islands
(count:183)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:71566408-71566651	K562	blood:	n/a	n/a
2	ARID3A	chr7:71617750-71618104	HepG2	liver:	n/a	n/a
3	ATF1	chr7:71566508-71566836	K562	blood:	n/a	n/a
4	ATF2	chr7:71730494-71730993	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:71730568-71730921	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:71676233-71676530	K562	blood:	n/a	n/a
7	BACH1	chr7:71676169-71676646	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr7:71635548-71635785	GM12878	blood:	n/a	n/a
9	BATF	chr7:71674059-71674398	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:71674079-71674389	GM12878	blood:	n/a	n/a
11	BCL3	chr7:71684529-71684809	GM12878	blood:	n/a	n/a
12	BHLHE40	chr7:71566539-71566915	K562	blood:	n/a	n/a
13	BHLHE40	chr7:71730295-71730461	K562	blood:	n/a	n/a
14	BHLHE40	chr7:71588969-71589244	HepG2	liver:	n/a	n/a
15	BHLHE40	chr7:71617595-71618001	HepG2	liver:	n/a	n/a
16	CCNT2	chr7:71566482-71566783	K562	blood:	n/a	n/a
17	CEBPB	chr7:71723050-71723323	A549	lung:	n/a	chr7:71723174-71723185
18	CEBPB	chr7:71721022-71721087	HepG2	liver:	n/a	chr7:71721064-71721077
19	CEBPB	chr7:71723120-71723245	K562	blood:	n/a	chr7:71723174-71723185
20	CEBPB	chr7:71672394-71672528	HepG2	liver:	n/a	n/a
21	CEBPB	chr7:71668950-71669066	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:71723021-71723355	HepG2	liver:	n/a	chr7:71723174-71723185
23	CEBPB	chr7:71605123-71605311	K562	blood:	n/a	chr7:71605206-71605217
24	CEBPB	chr7:71711676-71711904	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:71652114-71652386	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:71711658-71711926	K562	blood:	n/a	n/a
27	CEBPB	chr7:71614550-71614874	HepG2	liver:	n/a	chr7:71614702-71614713
28	CEBPB	chr7:71605041-71605227	A549	lung:	n/a	chr7:71605206-71605217
29	CEBPB	chr7:71630836-71631036	HepG2	liver:	n/a	chr7:71630947-71630956 chr7:71630946-71630957 chr7:71630945-71630956
30	CEBPB	chr7:71605024-71605315	HepG2	liver:	n/a	chr7:71605206-71605217
31	CEBPB	chr7:71723036-71723330	IMR90	lung:	n/a	chr7:71723174-71723185
32	CEBPB	chr7:71614594-71614788	K562	blood:	n/a	chr7:71614702-71614713
33	CEBPB	chr7:71729286-71729372	HepG2	liver:	n/a	chr7:71729324-71729335
34	CEBPD	chr7:71566329-71566957	K562	blood:	n/a	n/a
35	CEBPD	chr7:71566388-71566939	K562	blood:	n/a	n/a
36	CHD2	chr7:71722105-71722245	K562	blood:	n/a	n/a
37	CREB1	chr7:71626644-71626968	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr7:71626660-71626810	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr7:71648905-71649122	Medullo	brain:	n/a	chr7:71649005-71649026 chr7:71649003-71649021 chr7:71649004-71649020 chr7:71649006-71649015
40	CTCF	chr7:71564000-71564150	AG04449	skin:	n/a	n/a
41	CTCF	chr7:71626555-71626934	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr7:71626700-71626850	HepG2	liver:	n/a	n/a
43	CTCF	chr7:71626559-71626864	K562	blood:	n/a	n/a
44	CTCF	chr7:71734401-71734427	Lung_OC	lung:	n/a	n/a
45	CTCF	chr7:71626600-71626750	A549	lung:	n/a	n/a
46	CTCF	chr7:71626696-71626804	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:71648980-71649130	GM06990	blood:	n/a	chr7:71649005-71649026 chr7:71649003-71649021 chr7:71649004-71649020 chr7:71649006-71649015
48	CTCF	chr7:71724171-71724188	GM13976	blood:	n/a	n/a
49	CTCF	chr7:71626565-71626918	K562	blood:	n/a	n/a
50	CTCF	chr7:71648960-71649110	GM12872	blood:	n/a	chr7:71649005-71649026 chr7:71649003-71649021 chr7:71649004-71649020 chr7:71649006-71649015

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71729065-71729115	GM12892	blood:	n/a
2	chr7:71682306-71682356	NHDF-neo	bronchial:	n/a
3	chr7:71729065-71729115	T-47D	breast:	n/a
4	chr7:71729065-71729115	NHDF-neo	bronchial:	n/a
5	chr7:71682306-71682356	GM06990	blood:	n/a
6	chr7:71682306-71682356	SK-N-MC	brain:	n/a
7	chr7:71729065-71729115	HEEpiC	esophagus:	n/a
8	chr7:71578347-71578397	LNCaP	prostate:	n/a
9	chr7:71682306-71682356	CMK	blood:	n/a
10	chr7:71729065-71729115	Jurkat	blood:	n/a
11	chr7:71729065-71729115	NB4	blood:	n/a
12	chr7:71682306-71682356	HepG2	liver:	n/a
13	chr7:71578347-71578397	HEEpiC	esophagus:	n/a
14	chr7:71729065-71729115	AG10803	skin:	n/a
15	chr7:71729065-71729115	HL-60	blood:	n/a
16	chr7:71578347-71578397	AG04449	skin:	fetal
17	chr7:71682306-71682356	AG04450	lung:	fetal
18	chr7:71729065-71729115	MCF-7	breast:	n/a
19	chr7:71578347-71578397	NHBE	bronchial:	n/a
20	chr7:71578347-71578397	PANC-1	pancreas:	n/a
21	chr7:71578347-71578397	HUVEC	blood vessel:	n/a
22	chr7:71682306-71682356	PFSK-1	brain:	n/a
23	chr7:71729065-71729115	ovcar-3	ovarian:	n/a
24	chr7:71729065-71729115	HCT-116	colon:	n/a
25	chr7:71729065-71729115	GM06990	blood:	n/a
26	chr7:71729065-71729115	PrEC	prostate:	n/a
27	chr7:71729065-71729115	BJ	skin:	n/a
28	chr7:71682306-71682356	NHBE	bronchial:	n/a
29	chr7:71682306-71682356	Jurkat	blood:	n/a
30	chr7:71729065-71729115	HAEpiC	amniotic membrane:	n/a
31	chr7:71729065-71729115	PFSK-1	brain:	n/a
32	chr7:71729065-71729115	BE2_C	brain:	n/a
33	chr7:71578347-71578397	U87	brain:	n/a
34	chr7:71682306-71682356	HEK293	kidney:	embryo
35	chr7:71682306-71682356	ECC-1	luminal epithelium:	n/a
36	chr7:71729065-71729115	ProgFib	skin:	n/a
37	chr7:71682306-71682356	HCM	heart:	n/a
38	chr7:71578347-71578397	SAEC	small airway:	n/a
39	chr7:71729065-71729115	HCF	heart:	n/a
40	chr7:71578347-71578397	GM06990	blood:	n/a
41	chr7:71578347-71578397	HMEC	breast:	n/a
42	chr7:71729065-71729115	GM19239	blood:	n/a
43	chr7:71578347-71578397	PrEC	prostate:	n/a
44	chr7:71682306-71682356	GM19239	blood:	n/a
45	chr7:71729065-71729115	AoSMC	blood vessel:	n/a
46	chr7:71578347-71578397	NB4	blood:	n/a
47	chr7:71578347-71578397	SK-N-SH	brain:	n/a
48	chr7:71578347-71578397	HCF	heart:	n/a
49	chr7:71682306-71682356	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:71682306-71682356	ProgFib	skin:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
2	chr7:71593896..71596339-chr7:71598361..71599867,2	K562	blood:
3	chr7:71721716..71724334-chr7:71739335..71741214,2	K562	blood:
4	chr7:71642905..71645487-chr7:71655969..71658022,2	K562	blood:
5	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:
6	chr7:71663421..71665320-chr7:71669615..71672136,2	K562	blood:
7	chr7:71721877..71723519-chr7:71725703..71728534,2	K562	blood:
8	chr7:71642905..71645487-chr7:71655969..71658022,2	K562	blood:
9	chr7:71730756..71733410-chr7:71737455..71739236,2	K562	blood:
10	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
11	chr7:71593896..71596339-chr7:71598361..71599867,2	K562	blood:
12	chr7:71724576..71726876-chr7:71731815..71733875,3	K562	blood:
13	chr7:71628262..71630650-chr7:71934094..71936911,2	K562	blood:
14	chr7:71698392..71700394-chr7:71705051..71707157,2	K562	blood:
15	chr7:71663421..71665320-chr7:71669615..71672136,2	K562	blood:
16	chr7:71648521..71649566-chr7:71958858..71959802,3	MCF-7	breast:
17	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
18	chr7:71698392..71700394-chr7:71705051..71707157,2	K562	blood:
19	chr7:71549650..71551366-chr7:71562854..71564713,2	K562	blood:
20	chr7:71585300..71586969-chr7:71589158..71591405,2	K562	blood:
21	chr7:71586492..71588717-chr7:71593112..71596072,2	K562	blood:
22	chr1:64494077..64494875-chr7:71705794..71706323,2	MCF-7	breast:

No data

Variant related genes	Relation type
ABCF2P2	TF binding region
ABCF2P2	CpG island
ENSG00000207190	chromatin interactions

Extended variants
information (count: 8525 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:8525 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138852481	chr7:71552191-71552192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182092258	chr7:71552192-71552193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186818309	chr7:71552241-71552242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142057662	chr7:71552263-71552264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549764484	chr7:71552343-71552344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146350345	chr7:71552370-71552371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371723085	chr7:71552425-71552426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560496441	chr7:71552434-71552435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532843010	chr7:71552486-71552487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547821182	chr7:71552491-71552492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73124374	chr7:71552515-71552516	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs536481790	chr7:71552528-71552529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369845449	chr7:71552558-71552559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548573576	chr7:71552580-71552581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs10252717	chr7:71552621-71552622	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569838788	chr7:71552652-71552653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75685656	chr7:71552699-71552700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571461919	chr7:71552708-71552709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13244640	chr7:71552709-71552710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558921229	chr7:71552725-71552726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537962585	chr7:71552727-71552728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577815422	chr7:71552734-71552735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538922028	chr7:71552736-71552737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs844725	chr7:71552785-71552786	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs572254050	chr7:71552795-71552796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542872070	chr7:71552811-71552812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78256357	chr7:71552817-71552818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576214640	chr7:71552844-71552845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543002499	chr7:71552859-71552860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs564893080	chr7:71552866-71552867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs149626698	chr7:71552873-71552874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548051771	chr7:71552874-71552875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559644769	chr7:71552880-71552881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551224673	chr7:71552886-71552887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571401104	chr7:71552958-71552959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548392793	chr7:71553031-71553032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569776727	chr7:71553043-71553044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117905290	chr7:71553054-71553055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35830920	chr7:71553068-71553069	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs144384707	chr7:71553069-71553070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs112974685	chr7:71553084-71553085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10950292	chr7:71553102-71553103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs113707212	chr7:71553106-71553107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555751485	chr7:71553125-71553126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572393434	chr7:71553166-71553167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73371704	chr7:71553193-71553194	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554806735	chr7:71553200-71553201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs576350903	chr7:71553211-71553212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148805687	chr7:71553276-71553277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538845935	chr7:71553349-71553350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
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
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:625 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71547800-71552400	Weak transcription	Thymus	Thymus
2	chr7:71547800-71552400	Weak transcription	Dnd41	blood
3	chr7:71548200-71552400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:71548800-71552800	Weak transcription	Fetal Thymus	thymus
5	chr7:71550200-71552400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr7:71552400-71553000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:71552400-71553000	Enhancers	Thymus	Thymus
8	chr7:71552400-71553400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:71552400-71553400	Enhancers	Dnd41	blood
10	chr7:71552600-71553400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr7:71552800-71553200	Enhancers	Fetal Thymus	thymus
12	chr7:71553000-71553400	Enhancers	Gastric	stomach
13	chr7:71553000-71555800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:71553000-71563000	Weak transcription	Thymus	Thymus
15	chr7:71553200-71559000	Weak transcription	Fetal Thymus	thymus
16	chr7:71553400-71555600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:71555600-71558600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:71556600-71557000	Enhancers	Fetal Brain Male	brain
19	chr7:71557800-71558400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
20	chr7:71558400-71572800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:71558600-71560800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:71559000-71559200	Enhancers	Brain Anterior Caudate	brain
23	chr7:71559000-71571400	Strong transcription	Fetal Thymus	thymus
24	chr7:71559200-71564000	Weak transcription	Brain Anterior Caudate	brain
25	chr7:71560400-71560800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:71560400-71560800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr7:71560600-71561000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr7:71560600-71561200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:71560800-71562400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:71561200-71573000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:71561400-71561600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:71561400-71561600	Enhancers	Pancreas	Pancrea
33	chr7:71561600-71568800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:71561600-71570800	Weak transcription	Pancreas	Pancrea
35	chr7:71562400-71563000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:71563000-71564000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:71563000-71564200	Strong transcription	Thymus	Thymus
38	chr7:71563200-71564000	Enhancers	Osteobl	bone
39	chr7:71563400-71563600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr7:71563400-71563800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:71563400-71563800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:71563400-71564000	Enhancers	NHDF-Ad	bronchial
43	chr7:71563400-71564400	Enhancers	Fetal Muscle Trunk	muscle
44	chr7:71563400-71565200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:71563600-71563800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:71563600-71563800	Enhancers	Adipose Nuclei	Adipose
47	chr7:71563600-71564200	Enhancers	Fetal Muscle Leg	muscle
48	chr7:71563800-71564000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:71563800-71564200	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr7:71563800-71564600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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