Variant report

Variant	nsv888344
Chromosome Location	chr7:71406392-71488833
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	ARID3A	chr7:71455218-71455241	K562	blood:	n/a	n/a
2	ATF1	chr7:71455137-71455357	K562	blood:	n/a	n/a
3	ATF1	chr7:71441751-71441900	K562	blood:	n/a	n/a
4	ATF3	chr7:71472043-71472292	K562	blood:	n/a	n/a
5	BHLHE40	chr7:71437671-71437780	K562	blood:	n/a	n/a
6	BHLHE40	chr7:71441707-71442056	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:71472048-71472269	HepG2	liver:	n/a	n/a
8	BHLHE40	chr7:71441508-71442071	K562	blood:	n/a	n/a
9	BHLHE40	chr7:71471980-71472347	K562	blood:	n/a	n/a
10	BHLHE40	chr7:71441760-71441968	HepG2	liver:	n/a	n/a
11	BHLHE40	chr7:71482409-71482546	K562	blood:	n/a	n/a
12	CEBPB	chr7:71452436-71452755	Hela-S3	cervix:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
13	CEBPB	chr7:71452403-71452765	IMR90	lung:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
14	CEBPB	chr7:71408037-71408250	A549	lung:	n/a	chr7:71408203-71408214
15	CEBPB	chr7:71452405-71452773	A549	lung:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
16	CEBPB	chr7:71417560-71417881	HepG2	liver:	n/a	chr7:71417710-71417721 chr7:71417708-71417721 chr7:71417708-71417719
17	CEBPB	chr7:71408057-71408276	K562	blood:	n/a	chr7:71408203-71408214
18	CEBPB	chr7:71452385-71452754	MCF-7	breast:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
19	CEBPB	chr7:71408031-71408368	HepG2	liver:	n/a	chr7:71408203-71408214
20	CEBPB	chr7:71452413-71452755	H1-hESC	embryonic stem cell:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
21	CEBPB	chr7:71417549-71417878	K562	blood:	n/a	chr7:71417710-71417721 chr7:71417708-71417721 chr7:71417708-71417719
22	CEBPB	chr7:71408069-71408273	IMR90	lung:	n/a	chr7:71408203-71408214
23	CEBPB	chr7:71452326-71452772	HepG2	liver:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
24	CEBPB	chr7:71486191-71486385	HepG2	liver:	n/a	chr7:71486210-71486221
25	CEBPB	chr7:71487571-71487779	HepG2	liver:	n/a	chr7:71487689-71487700 chr7:71487688-71487701 chr7:71487688-71487699
26	CEBPB	chr7:71452347-71452765	K562	blood:	n/a	chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452584-71452593 chr7:71452581-71452598
27	CHD2	chr7:71420087-71420348	K562	blood:	n/a	n/a
28	CTCF	chr7:71418028-71418067	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:71408900-71409050	HRE	kidney:	n/a	n/a
30	CTCF	chr7:71427300-71427450	GM12867	blood:	n/a	n/a
31	CTCF	chr7:71452942-71452948	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr7:71452957-71452965	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr7:71419283-71419305	GM10248	blood:	n/a	n/a
34	CTCF	chr7:71474589-71474646	GM13976	blood:	n/a	n/a
35	CUX1	chr7:71441688-71441826	K562	blood:	n/a	n/a
36	E2F4	chr7:71423641-71423697	MCF10A-Er-Src	breast:	n/a	n/a
37	EGR1	chr7:71455172-71455412	K562	blood:	n/a	n/a
38	EGR1	chr7:71455213-71455394	K562	blood:	n/a	n/a
39	HCFC1	chr7:71455218-71455284	K562	blood:	n/a	n/a
40	HCFC1	chr7:71472039-71472251	K562	blood:	n/a	n/a
41	JUN	chr7:71454538-71455182	K562	blood:	n/a	chr7:71454695-71454704
42	JUND	chr7:71476765-71476967	HepG2	liver:	n/a	chr7:71476897-71476908
43	JUND	chr7:71454898-71455364	K562	blood:	n/a	n/a
44	JUND	chr7:71417869-71418062	K562	blood:	n/a	chr7:71417930-71417938 chr7:71417929-71417939
45	JUND	chr7:71431937-71432472	HepG2	liver:	n/a	chr7:71432343-71432354
46	JUND	chr7:71476817-71476967	K562	blood:	n/a	chr7:71476897-71476908
47	JUND	chr7:71441455-71442040	K562	blood:	n/a	n/a
48	MAFF	chr7:71482502-71482640	HepG2	liver:	n/a	n/a
49	MAFF	chr7:71417955-71418006	K562	blood:	n/a	n/a
50	MAFK	chr7:71482437-71482692	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:71407390-71407440	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:71407390-71407440	BJ	skin:	n/a
3	chr7:71407390-71407440	SK-N-SH	brain:	n/a
4	chr7:71407448-71407498	NHDF-neo	bronchial:	n/a
5	chr7:71407448-71407498	SAEC	small airway:	n/a
6	chr7:71407448-71407498	PFSK-1	brain:	n/a
7	chr7:71407306-71407356	AoSMC	blood vessel:	n/a
8	chr7:71407390-71407440	AG10803	skin:	n/a
9	chr7:71407448-71407498	Hela-S3	cervix:	n/a
10	chr7:71407390-71407440	SK-N-SH_RA	brain:	n/a
11	chr7:71407448-71407498	SK-N-SH_RA	brain:	n/a
12	chr7:71407390-71407440	PFSK-1	brain:	n/a
13	chr7:71407306-71407356	HCT-116	colon:	n/a
14	chr7:71407390-71407440	Jurkat	blood:	n/a
15	chr7:71407448-71407498	HNPCEpiC	eye:	n/a
16	chr7:71407448-71407498	HEEpiC	esophagus:	n/a
17	chr7:71407306-71407356	NHBE	bronchial:	n/a
18	chr7:71407448-71407498	HRE	kidney:	n/a
19	chr7:71407390-71407440	Caco-2	colon:	n/a
20	chr7:71407306-71407356	SAEC	small airway:	n/a
21	chr7:71407306-71407356	ovcar-3	ovarian:	n/a
22	chr7:71407390-71407440	AG09319	gingival:	n/a
23	chr7:71407390-71407440	Hepatocyte	liver:	n/a
24	chr7:71407448-71407498	HRCEpiC	kidney:	n/a
25	chr7:71407306-71407356	NT2-D1	testis:	n/a
26	chr7:71407390-71407440	AG04449	skin:	fetal
27	chr7:71407448-71407498	GM12891	blood:	n/a
28	chr7:71407306-71407356	HAEpiC	amniotic membrane:	n/a
29	chr7:71407306-71407356	HRPEpiC	eye:	n/a
30	chr7:71407448-71407498	A549	lung:	n/a
31	chr7:71407306-71407356	MCF-7	breast:	n/a
32	chr7:71407448-71407498	AG04449	skin:	fetal
33	chr7:71407390-71407440	A549	lung:	n/a
34	chr7:71407306-71407356	HCPEpiC	choroid plexus:	n/a
35	chr7:71407306-71407356	GM06990	blood:	n/a
36	chr7:71407390-71407440	CMK	blood:	n/a
37	chr7:71407448-71407498	BE2_C	brain:	n/a
38	chr7:71407390-71407440	MCF-7	breast:	n/a
39	chr7:71407448-71407498	HepG2	liver:	n/a
40	chr7:71407448-71407498	HAEpiC	amniotic membrane:	n/a
41	chr7:71407448-71407498	IMR90	lung:	fetal
42	chr7:71407390-71407440	HNPCEpiC	eye:	n/a
43	chr7:71407306-71407356	PrEC	prostate:	n/a
44	chr7:71407448-71407498	NB4	blood:	n/a
45	chr7:71407448-71407498	CMK	blood:	n/a
46	chr7:71407448-71407498	AG09309	skin:	n/a
47	chr7:71407306-71407356	PFSK-1	brain:	n/a
48	chr7:71407448-71407498	GM12892	blood:	n/a
49	chr7:71407390-71407440	HepG2	liver:	n/a
50	chr7:71407448-71407498	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:71430764..71432829-chr7:71445344..71447656,2	K562	blood:
2	chr7:71452826..71454470-chr7:71455028..71457199,2	MCF-7	breast:
3	chr7:71452826..71454470-chr7:71455028..71457199,2	MCF-7	breast:
4	chr6:30851925..30854155-chr7:71462779..71465346,2	MCF-7	breast:
5	chr7:71430764..71432829-chr7:71445344..71447656,2	K562	blood:

Variant related genes	Relation type
ENSG00000235581	TF binding region
ENSG00000235581	CpG island
ENSG00000204580	chromatin interactions

Extended variants
information (count: 3456 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3456 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10271976	chr7:71406392-71406393	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185513353	chr7:71406424-71406425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557771587	chr7:71406430-71406431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572899776	chr7:71406477-71406478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558221456	chr7:71406499-71406500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540356115	chr7:71406545-71406546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561831885	chr7:71406569-71406570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371668817	chr7:71406576-71406577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545092736	chr7:71406620-71406621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74894929	chr7:71406674-71406675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542031594	chr7:71406715-71406716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563295643	chr7:71406743-71406744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375932342	chr7:71406762-71406763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138481432	chr7:71406789-71406790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188700378	chr7:71406812-71406813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367624325	chr7:71406818-71406819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs36046543	chr7:71406823-71406824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528070171	chr7:71406837-71406838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142498769	chr7:71406840-71406841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112689910	chr7:71406854-71406855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377262505	chr7:71406861-71406862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115557585	chr7:71406870-71406871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34557765	chr7:71406908-71406909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180843351	chr7:71406911-71406912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574169145	chr7:71406921-71406922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372005426	chr7:71406924-71406925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566563331	chr7:71406965-71406966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11981933	chr7:71407001-71407002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs555315519	chr7:71407045-71407046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574084963	chr7:71407086-71407087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369777708	chr7:71407111-71407112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557158081	chr7:71407118-71407119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575340841	chr7:71407121-71407122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141430508	chr7:71407135-71407136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150820728	chr7:71407144-71407145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528360027	chr7:71407166-71407167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563042981	chr7:71407206-71407207	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186195867	chr7:71407209-71407210	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191914212	chr7:71407229-71407230	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528993351	chr7:71407238-71407239	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184101590	chr7:71407242-71407243	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374312391	chr7:71407258-71407259	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373643565	chr7:71407259-71407260	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544600431	chr7:71407288-71407289	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564567381	chr7:71407306-71407307	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569463427	chr7:71407318-71407319	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185974031	chr7:71407323-71407324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551526827	chr7:71407334-71407335	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76645505	chr7:71407359-71407360	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534178696	chr7:71407362-71407363	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71399800-71407400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:71399800-71407400	Weak transcription	Fetal Thymus	thymus
3	chr7:71400400-71424400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr7:71401200-71431000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:71401400-71407200	Weak transcription	Thymus	Thymus
6	chr7:71401800-71407200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:71403400-71431000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:71407200-71408000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:71407200-71408000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:71407200-71409200	Strong transcription	Thymus	Thymus
11	chr7:71407400-71408200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr7:71407400-71408200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:71407400-71408200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:71407400-71409400	Strong transcription	Fetal Thymus	thymus
15	chr7:71408000-71408200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr7:71408000-71416800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:71408000-71430800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:71408800-71409000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:71409200-71419400	Weak transcription	Thymus	Thymus
20	chr7:71409400-71430800	Weak transcription	Fetal Thymus	thymus
21	chr7:71416800-71417800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:71416800-71418200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr7:71417000-71417600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr7:71417000-71417800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr7:71417200-71417600	Enhancers	H9 Cell Line	embryonic stem cell
26	chr7:71417200-71417600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr7:71417200-71417600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:71417200-71418000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr7:71417200-71418000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr7:71418200-71420000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr7:71419400-71420400	Strong transcription	Thymus	Thymus
32	chr7:71420400-71423400	Weak transcription	Thymus	Thymus
33	chr7:71423400-71424000	Strong transcription	Thymus	Thymus
34	chr7:71424000-71430800	Weak transcription	Thymus	Thymus
35	chr7:71427600-71427800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:71428000-71429000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:71428800-71429000	Enhancers	Brain Hippocampus Middle	brain
38	chr7:71428800-71429600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr7:71429000-71429200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:71429000-71429200	Flanking Active TSS	Brain Hippocampus Middle	brain
41	chr7:71429000-71429200	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr7:71429000-71429200	Active TSS	Brain Substantia Nigra	brain
43	chr7:71429000-71429400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr7:71429000-71429400	Enhancers	Brain Angular Gyrus	brain
45	chr7:71429000-71429400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr7:71429000-71429400	Enhancers	Fetal Brain Female	brain
47	chr7:71429200-71429400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:71429200-71429400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
49	chr7:71429200-71429600	Active TSS	Brain Cingulate Gyrus	brain
50	chr7:71429200-71429600	Active TSS	Brain Hippocampus Middle	brain

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