Variant report

Variant	nsv966872
Chromosome Location	chr7:102791751-102798505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102792428-102792755	HepG2	liver:	n/a	n/a
2	ATF1	chr7:102792752-102793085	K562	blood:	n/a	n/a
3	CCNT2	chr7:102792898-102793049	K562	blood:	n/a	n/a
4	CEBPB	chr7:102793027-102793095	HepG2	liver:	n/a	chr7:102793062-102793073
5	CEBPB	chr7:102792920-102793032	K562	blood:	n/a	n/a
6	CUX1	chr7:102792920-102793059	K562	blood:	n/a	n/a
7	EBF1	chr7:102795744-102796474	GM12878	blood:	n/a	chr7:102795999-102796010
8	EBF1	chr7:102795806-102796232	GM12878	blood:	n/a	chr7:102795999-102796010
9	EBF1	chr7:102795725-102796440	GM12878	blood:	n/a	chr7:102795999-102796010
10	EP300	chr7:102792768-102793123	K562	blood:	n/a	n/a
11	FOXA1	chr7:102794510-102794766	HepG2	liver:	n/a	chr7:102794649-102794664
12	FOXA1	chr7:102794493-102794852	HepG2	liver:	n/a	chr7:102794649-102794664
13	FOXA1	chr7:102794489-102794765	HepG2	liver:	n/a	chr7:102794649-102794664
14	FOXA1	chr7:102794513-102794879	HepG2	liver:	n/a	chr7:102794649-102794664
15	FOXA1	chr7:102792301-102792775	HepG2	liver:	n/a	n/a
16	FOXA2	chr7:102794534-102794735	HepG2	liver:	n/a	n/a
17	GATA1	chr7:102792295-102793303	PBDE	blood:	n/a	n/a
18	GATA2	chr7:102792438-102793121	K562	blood:	n/a	n/a
19	HDAC2	chr7:102793631-102794149	K562	blood:	n/a	n/a
20	HDAC2	chr7:102793770-102794072	K562	blood:	n/a	n/a
21	HNF4A	chr7:102792391-102792817	HepG2	liver:	n/a	chr7:102792600-102792615
22	HNF4A	chr7:102792462-102792805	HepG2	liver:	n/a	chr7:102792600-102792615
23	HNF4G	chr7:102792397-102792784	HepG2	liver:	n/a	chr7:102792601-102792616
24	IRF1	chr7:102796084-102796374	K562	blood:	n/a	n/a
25	IRF1	chr7:102796154-102796212	K562	blood:	n/a	n/a
26	IRF4	chr7:102795999-102796369	GM12878	blood:	n/a	n/a
27	IRF4	chr7:102795912-102796413	GM12878	blood:	n/a	n/a
28	JUN	chr7:102792841-102793086	K562	blood:	n/a	n/a
29	JUND	chr7:102792755-102793123	K562	blood:	n/a	n/a
30	MAFF	chr7:102792422-102792567	K562	blood:	n/a	chr7:102792491-102792509
31	MAFF	chr7:102792327-102792655	HepG2	liver:	n/a	chr7:102792491-102792509
32	MAFK	chr7:102792331-102792655	HepG2	liver:	n/a	chr7:102792492-102792507
33	MAFK	chr7:102792317-102792668	HepG2	liver:	n/a	chr7:102792492-102792507
34	MAX	chr7:102796325-102796341	GM12878	blood:	n/a	n/a
35	MTA3	chr7:102795982-102796525	GM12878	blood:	n/a	n/a
36	MXI1	chr7:102796096-102796343	GM12878	blood:	n/a	n/a
37	MYBL2	chr7:102792260-102792834	HepG2	liver:	n/a	n/a
38	NFYB	chr7:102793178-102793377	K562	blood:	n/a	n/a
39	NR2F2	chr7:102791501-102792077	MCF-7	breast:	n/a	n/a
40	NR2F2	chr7:102792749-102793130	K562	blood:	n/a	n/a
41	NR2F2	chr7:102791435-102792000	MCF-7	breast:	n/a	n/a
42	PAX5	chr7:102796071-102796445	GM12878	blood:	n/a	n/a
43	PAX5	chr7:102796015-102796352	GM12878	blood:	n/a	n/a
44	POLR2A	chr7:102793295-102793460	Gliobla	brain:	n/a	n/a
45	POLR2A	chr7:102798162-102798558	K562	blood:	n/a	n/a
46	POLR2A	chr7:102796048-102796460	GM12878	blood:	n/a	n/a
47	POLR2A	chr7:102793138-102793759	PANC-1	pancreas:	n/a	n/a
48	POLR2A	chr7:102793278-102793294	Gliobla	brain:	n/a	n/a
49	POLR2A	chr7:102796136-102796326	K562	blood:	n/a	n/a
50	POLR2A	chr7:102793183-102793532	PANC-1	pancreas:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102793411-102793461	ECC-1	luminal epithelium:	n/a
2	chr7:102793411-102793461	HRPEpiC	eye:	n/a
3	chr7:102792783-102792833	NH-A	brain:	n/a
4	chr7:102792783-102792833	HRCEpiC	kidney:	n/a
5	chr7:102793411-102793461	HAEpiC	amniotic membrane:	n/a
6	chr7:102793411-102793461	Hela-S3	cervix:	n/a
7	chr7:102793411-102793461	T-47D	breast:	n/a
8	chr7:102792783-102792833	GM12891	blood:	n/a
9	chr7:102792783-102792833	HL-60	blood:	n/a
10	chr7:102792783-102792833	HCT-116	colon:	n/a
11	chr7:102793411-102793461	H1-hESC	embryonic stem cell:	embryo
12	chr7:102792783-102792833	NT2-D1	testis:	n/a
13	chr7:102792783-102792833	PFSK-1	brain:	n/a
14	chr7:102793411-102793461	ovcar-3	ovarian:	n/a
15	chr7:102793411-102793461	HepG2	liver:	n/a
16	chr7:102793411-102793461	HUVEC	blood vessel:	n/a
17	chr7:102793411-102793461	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:102793411-102793461	ProgFib	skin:	n/a
19	chr7:102793411-102793461	GM19239	blood:	n/a
20	chr7:102792783-102792833	RPTEC	kidney:	n/a
21	chr7:102793411-102793461	HIPEpiC	eye:	n/a
22	chr7:102793411-102793461	HCPEpiC	choroid plexus:	n/a
23	chr7:102793411-102793461	GM12878	blood:	n/a
24	chr7:102792783-102792833	CMK	blood:	n/a
25	chr7:102793411-102793461	BE2_C	brain:	n/a
26	chr7:102792783-102792833	GM12892	blood:	n/a
27	chr7:102793411-102793461	BJ	skin:	n/a
28	chr7:102792783-102792833	HEEpiC	esophagus:	n/a
29	chr7:102793411-102793461	CMK	blood:	n/a
30	chr7:102793411-102793461	HCT-116	colon:	n/a
31	chr7:102793411-102793461	MCF10A-Er-Src	breast:	n/a
32	chr7:102793411-102793461	A549	lung:	n/a
33	chr7:102792783-102792833	H1-hESC	embryonic stem cell:	embryo
34	chr7:102792783-102792833	AG10803	skin:	n/a
35	chr7:102793411-102793461	AG04449	skin:	fetal
36	chr7:102793411-102793461	K562	blood:	n/a
37	chr7:102792783-102792833	SKMC	muscle:	n/a
38	chr7:102793411-102793461	LNCaP	prostate:	n/a
39	chr7:102792783-102792833	GM19239	blood:	n/a
40	chr7:102792783-102792833	HCM	heart:	n/a
41	chr7:102792783-102792833	HCPEpiC	choroid plexus:	n/a
42	chr7:102792783-102792833	AG04450	lung:	fetal
43	chr7:102792783-102792833	Caco-2	colon:	n/a
44	chr7:102792783-102792833	PANC-1	pancreas:	n/a
45	chr7:102793411-102793461	Caco-2	colon:	n/a
46	chr7:102793411-102793461	RPTEC	kidney:	n/a
47	chr7:102792783-102792833	AG09309	skin:	n/a
48	chr7:102792783-102792833	U87	brain:	n/a
49	chr7:102793411-102793461	HEEpiC	esophagus:	n/a
50	chr7:102792783-102792833	Jurkat	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102714725..102717201-chr7:102788241..102791780,5	K562	blood:
2	chr7:102784051..102785716-chr7:102793385..102795157,2	K562	blood:
3	chr7:102713709..102715211-chr7:102789642..102791984,2	K562	blood:
4	chr7:35082428..35085221-chr7:102798030..102799593,2	MCF-7	breast:
5	chr7:102733228..102736205-chr7:102789279..102791780,2	MCF-7	breast:
6	chr7:102787455..102790640-chr7:102797727..102800221,5	K562	blood:
7	chr7:102759379..102762894-chr7:102787802..102793821,6	K562	blood:
8	chr7:102714022..102717631-chr7:102788669..102792237,6	MCF-7	breast:
9	chr7:102790144..102791929-chr7:102937725..102939474,2	MCF-7	breast:
10	chr7:102789269..102791743-chr7:102791840..102795059,5	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NAPEPLD-2	chr7:102792454-102792486	NONHSAT122538
2	lnc-NAPEPLD-2	chr7:102792541-102792772	NONHSAT122538

No data

Variant related genes	Relation type
NAPEPLD	TF binding region
ENSG00000236848	TF binding region
NAPEPLD	CpG island
ENSG00000236848	CpG island
ENSG00000161040	chromatin interactions
ENSG00000105819	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000161048	chromatin interactions

Extended variants
information (count: 289 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567470322	chr7:102791783-102791784	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs537722624	chr7:102791807-102791808	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs11760826	chr7:102791811-102791812	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs374390873	chr7:102791841-102791842	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs148450522	chr7:102791845-102791846	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs538621011	chr7:102791856-102791857	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs142883629	chr7:102791867-102791868	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs572147251	chr7:102791903-102791904	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs542776122	chr7:102791907-102791908	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs377470104	chr7:102791910-102791911	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs77308183	chr7:102791920-102791921	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs10255884	chr7:102791925-102791926	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs574196317	chr7:102791926-102791927	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs142347377	chr7:102791933-102791934	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs563206127	chr7:102791982-102791983	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs150478412	chr7:102792003-102792004	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs138287972	chr7:102792019-102792020	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs181245968	chr7:102792055-102792056	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs115880270	chr7:102792140-102792141	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs549087438	chr7:102792141-102792142	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs186050517	chr7:102792145-102792146	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs538056870	chr7:102792174-102792175	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs553503153	chr7:102792194-102792195	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs62484774	chr7:102792272-102792273	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs571517159	chr7:102792285-102792286	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538960059	chr7:102792290-102792291	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs116285203	chr7:102792408-102792409	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572084191	chr7:102792427-102792428	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs143504875	chr7:102792451-102792452	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs554652435	chr7:102792479-102792480	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs28379145	chr7:102792518-102792519	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs11768467	chr7:102792550-102792551	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs544781617	chr7:102792579-102792580	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs562986853	chr7:102792584-102792585	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs578185947	chr7:102792585-102792586	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs541202595	chr7:102792648-102792649	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs565362938	chr7:102792680-102792681	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs532525026	chr7:102792707-102792708	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs544590835	chr7:102792721-102792722	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs527682995	chr7:102792750-102792751	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs116905697	chr7:102792758-102792759	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs115311350	chr7:102792762-102792763	Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs530372382	chr7:102792784-102792785	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs531760029	chr7:102792814-102792815	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs549928390	chr7:102792885-102792886	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs369425285	chr7:102792961-102792962	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs116769350	chr7:102792968-102792969	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs137913732	chr7:102793017-102793018	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs545992971	chr7:102793030-102793031	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs565630467	chr7:102793041-102793042	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21510904	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102790200-102792400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:102790200-102793600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:102790200-102793600	Enhancers	HepG2	liver
4	chr7:102790200-102803200	Weak transcription	Gastric	stomach
5	chr7:102790400-102791800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:102790400-102792000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:102790400-102792200	Enhancers	Small Intestine	intestine
8	chr7:102790400-102793000	Weak transcription	Aorta	Aorta
9	chr7:102790400-102793400	Weak transcription	Right Atrium	heart
10	chr7:102790400-102793600	Enhancers	Fetal Intestine Small	intestine
11	chr7:102790400-102794000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:102790400-102794000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr7:102790400-102796800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:102790600-102792600	Enhancers	Stomach Mucosa	stomach
15	chr7:102790600-102793200	Enhancers	Liver	Liver
16	chr7:102790800-102792200	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr7:102790800-102795600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr7:102790800-102795800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr7:102790800-102795800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr7:102790800-102796200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr7:102791000-102792200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr7:102791000-102792200	Weak transcription	Duodenum Mucosa	Duodenum
23	chr7:102791000-102792400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr7:102791000-102792400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr7:102791000-102794000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr7:102791000-102795600	Weak transcription	Brain Substantia Nigra	brain
27	chr7:102791000-102795800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr7:102791000-102795800	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr7:102791000-102795800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr7:102791000-102796200	Weak transcription	Spleen	Spleen
31	chr7:102791200-102791800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:102791200-102791800	Weak transcription	Brain Hippocampus Middle	brain
33	chr7:102791200-102794000	Weak transcription	GM12878-XiMat	blood
34	chr7:102791200-102794200	Enhancers	Fetal Intestine Large	intestine
35	chr7:102791200-102794800	Enhancers	K562	blood
36	chr7:102791400-102793000	Weak transcription	Cortex derived primary cultured neurospheres	brain
37	chr7:102791400-102793200	Weak transcription	Colonic Mucosa	Colon
38	chr7:102791600-102791800	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr7:102791600-102792400	Weak transcription	Brain Anterior Caudate	brain
40	chr7:102791800-102792000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:102791800-102792200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr7:102791800-102792400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr7:102791800-102792600	Enhancers	Brain Hippocampus Middle	brain
44	chr7:102792200-102792600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:102792200-102792600	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:102792200-102792600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
47	chr7:102792200-102792800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr7:102792200-102796000	Weak transcription	Small Intestine	intestine
49	chr7:102792400-102792600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:102792400-102792600	Enhancers	Brain Anterior Caudate	brain

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