Variant report

Variant	nsv519667
Chromosome Location	chr7:139969051-139992387
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:244)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:139974706-139975707	K562	blood:	n/a	n/a
2	ATF1	chr7:139974840-139975495	K562	blood:	n/a	n/a
3	BACH1	chr7:139975243-139975416	K562	blood:	n/a	n/a
4	BHLHE40	chr7:139974932-139975227	K562	blood:	n/a	n/a
5	CBX3	chr7:139970394-139971049	K562	blood:	n/a	n/a
6	CCNT2	chr7:139974825-139975516	K562	blood:	n/a	n/a
7	CEBPB	chr7:139975256-139975685	K562	blood:	n/a	chr7:139975505-139975518
8	CEBPB	chr7:139969069-139969330	HepG2	liver:	n/a	n/a
9	CEBPB	chr7:139985220-139985234	K562	blood:	n/a	n/a
10	CEBPB	chr7:139974823-139975603	K562	blood:	n/a	chr7:139975505-139975518
11	CEBPD	chr7:139974647-139975727	K562	blood:	n/a	n/a
12	CEBPD	chr7:139974721-139975315	K562	blood:	n/a	n/a
13	CTCF	chr7:139976395-139976440	LNCaP	prostate:	n/a	n/a
14	CTCF	chr7:139977560-139977710	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:139974948-139975148	K562	blood:	n/a	n/a
16	CTCF	chr7:139984040-139984190	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr7:139989700-139989850	K562	blood:	n/a	n/a
18	CUX1	chr7:139974848-139975548	K562	blood:	n/a	n/a
19	CUX1	chr7:139969143-139969215	K562	blood:	n/a	n/a
20	E2F4	chr7:139986275-139986474	MCF10A-Er-Src	breast:	n/a	n/a
21	ELF1	chr7:139988998-139989267	K562	blood:	n/a	n/a
22	EP300	chr7:139974758-139975406	K562	blood:	n/a	chr7:139975236-139975250 chr7:139975237-139975251
23	EP300	chr7:139974696-139975664	K562	blood:	n/a	chr7:139975236-139975250 chr7:139975237-139975251
24	EP300	chr7:139975998-139976022	K562	blood:	n/a	n/a
25	EP300	chr7:139976901-139977096	K562	blood:	n/a	n/a
26	FOSL2	chr7:139983344-139983768	HepG2	liver:	n/a	chr7:139983557-139983568
27	FOSL2	chr7:139983344-139983763	HepG2	liver:	n/a	chr7:139983557-139983568
28	FOXA1	chr7:139969067-139969490	HepG2	liver:	n/a	n/a
29	FOXA1	chr7:139969089-139969337	HepG2	liver:	n/a	n/a
30	FOXA2	chr7:139969125-139969355	HepG2	liver:	n/a	n/a
31	GATA1	chr7:139974566-139975869	PBDE	blood:	n/a	chr7:139975465-139975475
32	GATA1	chr7:139974610-139976260	K562	blood:	n/a	chr7:139975465-139975475
33	GATA2	chr7:139974740-139975193	K562	blood:	n/a	n/a
34	GATA2	chr7:139974674-139975528	K562	blood:	n/a	chr7:139975465-139975475
35	GATA3	chr7:139975548-139975609	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr7:139978548-139978549	SH-SY5Y	brain:	n/a	n/a
37	HCFC1	chr7:139974966-139975559	K562	blood:	n/a	n/a
38	HMGN3	chr7:139974782-139975583	K562	blood:	n/a	n/a
39	HNF4A	chr7:139981141-139981419	HepG2	liver:	n/a	chr7:139981311-139981326
40	IRF1	chr7:139974768-139975572	K562	blood:	n/a	chr7:139975480-139975490 chr7:139975480-139975494
41	JUND	chr7:139983451-139983720	K562	blood:	n/a	chr7:139983556-139983567
42	JUND	chr7:139983435-139983653	HepG2	liver:	n/a	chr7:139983556-139983567
43	JUND	chr7:139983398-139983713	HepG2	liver:	n/a	chr7:139983556-139983567
44	JUND	chr7:139983375-139983713	HepG2	liver:	n/a	chr7:139983556-139983567
45	JUND	chr7:139974802-139975487	K562	blood:	n/a	n/a
46	KAP1	chr7:139974994-139975493	K562	blood:	n/a	n/a
47	MAFF	chr7:139974948-139975609	K562	blood:	n/a	n/a
48	MAFK	chr7:139982074-139982206	HepG2	liver:	n/a	n/a
49	MAFK	chr7:139974826-139975750	K562	blood:	n/a	chr7:139975257-139975266
50	MAFK	chr7:139982051-139982194	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:139991704-139991754	HMEC	breast:	n/a
2	chr7:139992322-139992372	U87	brain:	n/a
3	chr7:139991704-139991754	GM12892	blood:	n/a
4	chr7:139991704-139991754	GM12891	blood:	n/a
5	chr7:139992322-139992372	HMEC	breast:	n/a
6	chr7:139989127-139989177	NB4	blood:	n/a
7	chr7:139971436-139971486	AG09309	skin:	n/a
8	chr7:139971436-139971486	AG09319	gingival:	n/a
9	chr7:139989127-139989177	PrEC	prostate:	n/a
10	chr7:139991704-139991754	LNCaP	prostate:	n/a
11	chr7:139971436-139971486	Hepatocyte	liver:	n/a
12	chr7:139991704-139991754	SK-N-SH_RA	brain:	n/a
13	chr7:139971436-139971486	HRCEpiC	kidney:	n/a
14	chr7:139991704-139991754	SK-N-SH	brain:	n/a
15	chr7:139989127-139989177	CMK	blood:	n/a
16	chr7:139971436-139971486	NHDF-neo	bronchial:	n/a
17	chr7:139989127-139989177	T-47D	breast:	n/a
18	chr7:139992322-139992372	IMR90	lung:	fetal
19	chr7:139971436-139971486	H1-hESC	embryonic stem cell:	embryo
20	chr7:139989127-139989177	BJ	skin:	n/a
21	chr7:139971436-139971486	SKMC	muscle:	n/a
22	chr7:139992322-139992372	Jurkat	blood:	n/a
23	chr7:139991704-139991754	PrEC	prostate:	n/a
24	chr7:139992322-139992372	A549	lung:	n/a
25	chr7:139971436-139971486	HCPEpiC	choroid plexus:	n/a
26	chr7:139991704-139991754	AoSMC	blood vessel:	n/a
27	chr7:139989127-139989177	PANC-1	pancreas:	n/a
28	chr7:139992322-139992372	BJ	skin:	n/a
29	chr7:139991704-139991754	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:139992322-139992372	HEK293	kidney:	embryo
31	chr7:139989127-139989177	AG09319	gingival:	n/a
32	chr7:139991704-139991754	MCF10A-Er-Src	breast:	n/a
33	chr7:139992322-139992372	NHBE	bronchial:	n/a
34	chr7:139992322-139992372	PFSK-1	brain:	n/a
35	chr7:139992322-139992372	SK-N-SH_RA	brain:	n/a
36	chr7:139991704-139991754	HEK293	kidney:	embryo
37	chr7:139992322-139992372	MCF10A-Er-Src	breast:	n/a
38	chr7:139991704-139991754	AG09309	skin:	n/a
39	chr7:139989127-139989177	IMR90	lung:	fetal
40	chr7:139991704-139991754	T-47D	breast:	n/a
41	chr7:139971436-139971486	HRE	kidney:	n/a
42	chr7:139992322-139992372	LNCaP	prostate:	n/a
43	chr7:139971436-139971486	GM12891	blood:	n/a
44	chr7:139992322-139992372	H1-hESC	embryonic stem cell:	embryo
45	chr7:139989127-139989177	BE2_C	brain:	n/a
46	chr7:139989127-139989177	GM06990	blood:	n/a
47	chr7:139992322-139992372	HUVEC	blood vessel:	n/a
48	chr7:139991704-139991754	HIPEpiC	eye:	n/a
49	chr7:139991704-139991754	A549	lung:	n/a
50	chr7:139992322-139992372	NB4	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:139874893..139878777-chr7:139985874..139988097,3	K562	blood:
2	chr7:139969481..139972137-chr7:139976037..139978399,3	K562	blood:
3	chr7:139975596..139977412-chr7:140003455..140004991,2	K562	blood:
4	chr7:139980079..139982335-chr7:139989698..139991733,2	K562	blood:
5	chr7:139875096..139876841-chr7:139982229..139984952,2	K562	blood:
6	chr7:139970498..139972137-chr7:139976828..139978399,2	K562	blood:
7	chr7:139136536..139138784-chr7:139972292..139974609,2	K562	blood:
8	chr7:139875131..139878552-chr7:139963598..139970685,8	K562	blood:
9	chr7:139956370..139960163-chr7:139965506..139969520,3	K562	blood:
10	chr7:139875973..139878045-chr7:139985474..139988107,2	MCF-7	breast:
11	chr7:139980842..139982492-chr7:139983850..139985688,2	K562	blood:
12	chr7:139983287..139985167-chr7:140004183..140006498,2	K562	blood:
13	chr7:139970498..139972137-chr7:139976828..139978399,2	K562	blood:
14	chr7:139969481..139972137-chr7:139976037..139978399,3	K562	blood:
15	chr7:139975332..139977325-chr7:139988336..139989898,2	K562	blood:
16	chr7:139875096..139877350-chr7:139981549..139984952,3	K562	blood:
17	chr7:139876776..139878486-chr7:139973785..139976029,2	K562	blood:
18	chr7:139986364..139989240-chr7:139991314..139993388,2	K562	blood:
19	chr7:139876301..139878777-chr7:139985874..139988097,2	K562	blood:
20	chr7:139967905..139969636-chr7:139970125..139972118,2	MCF-7	breast:
21	chr7:139967905..139969636-chr7:139970125..139972118,2	MCF-7	breast:
22	chr7:139975332..139977325-chr7:139988336..139989898,2	K562	blood:
23	chr7:139876001..139878497-chr7:139973324..139976029,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB19-2	chr7:139982265-139982720	NONHSAT123671

No data

Variant related genes	Relation type
PPP1R2P6	TF binding region
ENSG00000270512	TF binding region
PPP1R2P6	CpG island
ENSG00000270512	CpG island
ENSG00000260231	chromatin interactions
ENSG00000241661	chromatin interactions
ENSG00000270512	chromatin interactions
ENSG00000006459	chromatin interactions

Extended variants
information (count: 920 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2471312	chr7:139969051-139969052	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186596269	chr7:139969055-139969056	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs12703676	chr7:139969089-139969090	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs563999830	chr7:139969164-139969165	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74952306	chr7:139969214-139969215	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543160933	chr7:139969273-139969274	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs560120176	chr7:139969309-139969310	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114296642	chr7:139969317-139969318	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs35319810	chr7:139969329-139969330	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76861738	chr7:139969338-139969339	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs2471311	chr7:139969350-139969351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs2429209	chr7:139969353-139969354	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189856092	chr7:139969387-139969388	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs371210157	chr7:139969413-139969414	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182074825	chr7:139969431-139969432	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs2429208	chr7:139969443-139969444	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185987588	chr7:139969476-139969477	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs376510094	chr7:139969497-139969498	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551000480	chr7:139969501-139969502	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572720434	chr7:139969555-139969556	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs2471310	chr7:139969581-139969582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs62491802	chr7:139969592-139969593	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536947702	chr7:139969594-139969595	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150854753	chr7:139969603-139969604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571101080	chr7:139969612-139969613	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs567364256	chr7:139969623-139969624	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535092934	chr7:139969667-139969668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs532471362	chr7:139969686-139969687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs547353616	chr7:139969701-139969702	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2471309	chr7:139969709-139969710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs578173328	chr7:139969733-139969734	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs149615074	chr7:139969735-139969736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs202000694	chr7:139969790-139969791	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs557082021	chr7:139969831-139969832	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2471308	chr7:139969849-139969850	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs537541743	chr7:139969854-139969855	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs13232218	chr7:139969875-139969876	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561507125	chr7:139969887-139969888	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528642822	chr7:139969892-139969893	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs577489583	chr7:139969995-139969996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34362774	chr7:139970007-139970008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs559012277	chr7:139970019-139970020	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532907477	chr7:139970073-139970074	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373840975	chr7:139970152-139970153	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541729112	chr7:139970155-139970156	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143982395	chr7:139970177-139970178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530797694	chr7:139970190-139970191	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2471307	chr7:139970202-139970203	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567593698	chr7:139970236-139970237	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534801273	chr7:139970237-139970238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139960200-139971000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:139960400-139969200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:139960400-139975200	Weak transcription	Right Atrium	heart
4	chr7:139965400-139973400	Weak transcription	HepG2	liver
5	chr7:139966600-139969600	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr7:139966600-139969600	Enhancers	Primary T killer memory cells from peripheral blood	blood
7	chr7:139966600-139969800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr7:139966600-139969800	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr7:139966600-139970000	Enhancers	Primary T cells fromperipheralblood	blood
10	chr7:139966600-139970200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr7:139966800-139969600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr7:139968600-139969400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr7:139968600-139969400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:139968800-139969200	Flanking Active TSS	Primary T cells from cord blood	blood
15	chr7:139968800-139969200	Enhancers	Liver	Liver
16	chr7:139968800-139969400	Enhancers	Thymus	Thymus
17	chr7:139968800-139969600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:139969000-139969400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr7:139969000-139969600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr7:139969000-139969800	Enhancers	Fetal Thymus	thymus
21	chr7:139969200-139969400	Enhancers	Primary hematopoietic stem cells	blood
22	chr7:139969200-139969800	Enhancers	Primary T cells from cord blood	blood
23	chr7:139969400-139974800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr7:139970800-139971800	Active TSS	Placenta	Placenta
25	chr7:139971000-139971400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:139971400-139973200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:139972400-139975000	Weak transcription	Fetal Intestine Small	intestine
28	chr7:139972600-139972800	Enhancers	Gastric	stomach
29	chr7:139973200-139973400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:139973200-139973600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr7:139973200-139973600	Enhancers	Pancreas	Pancrea
32	chr7:139973400-139973600	Enhancers	Gastric	stomach
33	chr7:139973400-139973600	Enhancers	HepG2	liver
34	chr7:139973600-139975000	Weak transcription	HepG2	liver
35	chr7:139974200-139974800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:139974600-139974800	Enhancers	Adipose Nuclei	Adipose
37	chr7:139974600-139974800	Enhancers	K562	blood
38	chr7:139974800-139975000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:139974800-139975000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:139974800-139975000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr7:139974800-139975000	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr7:139974800-139975200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:139974800-139975600	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr7:139974800-139976000	Flanking Active TSS	K562	blood
45	chr7:139974800-139976200	Enhancers	Fetal Heart	heart
46	chr7:139974800-139977000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:139975000-139975200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:139975000-139975200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:139975000-139975200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr7:139975000-139975200	Enhancers	HepG2	liver

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