Variant report

Variant	nsv1026448
Chromosome Location	chr7:140636599-140716829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1532)
CpG islands
(count:1226)
Chromatin interactive
region (count:113)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1532 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:140701376-140701890	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:140683697-140683887	K562	blood:	n/a	n/a
3	ARID3A	chr7:140672793-140673511	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:140713904-140715185	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:140703154-140703586	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:140688819-140689290	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:140675727-140676180	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:140714267-140715024	K562	blood:	n/a	n/a
9	ATF1	chr7:140714313-140715084	K562	blood:	n/a	n/a
10	ATF2	chr7:140714359-140715143	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr7:140714231-140715048	GM12878	blood:	n/a	n/a
12	ATF2	chr7:140714214-140715005	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr7:140714118-140715335	GM12878	blood:	n/a	n/a
14	ATF3	chr7:140714454-140715107	A549	lung:	n/a	n/a
15	ATF3	chr7:140714137-140715080	A549	lung:	n/a	n/a
16	BACH1	chr7:140714381-140715169	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:140703479-140703637	K562	blood:	n/a	n/a
18	BCL3	chr7:140714246-140715110	A549	lung:	n/a	chr7:140714918-140714927
19	BCL3	chr7:140714333-140715178	A549	lung:	n/a	chr7:140714918-140714927
20	BCLAF1	chr7:140711847-140712230	GM12878	blood:	n/a	n/a
21	BCLAF1	chr7:140714111-140715103	GM12878	blood:	n/a	chr7:140714918-140714927
22	BCLAF1	chr7:140714192-140715104	GM12878	blood:	n/a	chr7:140714918-140714927
23	BHLHE40	chr7:140673304-140673308	A549	lung:	n/a	n/a
24	BHLHE40	chr7:140714399-140714914	A549	lung:	n/a	n/a
25	BHLHE40	chr7:140714128-140715439	K562	blood:	n/a	chr7:140714918-140714934
26	BHLHE40	chr7:140714306-140715163	GM12878	blood:	n/a	chr7:140714918-140714934
27	BHLHE40	chr7:140691868-140691980	K562	blood:	n/a	n/a
28	BRCA1	chr7:140673551-140673692	GM12878	blood:	n/a	n/a
29	BRCA1	chr7:140714351-140714993	GM12878	blood:	n/a	n/a
30	BRCA1	chr7:140714681-140714973	HepG2	liver:	n/a	n/a
31	BRCA1	chr7:140714279-140714958	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr7:140713886-140715463	K562	blood:	n/a	n/a
33	CBX3	chr7:140714115-140715406	K562	blood:	n/a	n/a
34	CBX3	chr7:140683652-140684106	K562	blood:	n/a	n/a
35	CBX3	chr7:140683611-140683955	K562	blood:	n/a	n/a
36	CBX3	chr7:140714054-140715289	HCT-116	colon:	n/a	n/a
37	CCNT2	chr7:140664038-140664045	K562	blood:	n/a	n/a
38	CCNT2	chr7:140714352-140715114	K562	blood:	n/a	n/a
39	CEBPB	chr7:140677607-140677928	MCF-7	breast:	n/a	chr7:140677827-140677839 chr7:140677717-140677728
40	CEBPB	chr7:140699926-140700177	K562	blood:	n/a	n/a
41	CEBPB	chr7:140680472-140680699	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:140666721-140666882	HepG2	liver:	n/a	chr7:140666816-140666827
43	CEBPB	chr7:140701414-140701591	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:140703933-140704094	HepG2	liver:	n/a	chr7:140704050-140704061
45	CEBPB	chr7:140672822-140673623	HepG2	liver:	n/a	chr7:140673085-140673098 chr7:140673085-140673096 chr7:140672976-140672987
46	CEBPB	chr7:140714230-140715351	GM12878	blood:	n/a	n/a
47	CEBPB	chr7:140698532-140698903	HepG2	liver:	n/a	chr7:140698706-140698717
48	CEBPB	chr7:140673284-140673546	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:140679845-140680090	A549	lung:	n/a	chr7:140679962-140679973
50	CEBPB	chr7:140714226-140715132	A549	lung:	n/a	n/a

(count:1226 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:140714661-140714711	Caco-2	colon:	n/a
2	chr7:140714661-140714711	Hela-S3	cervix:	n/a
3	chr7:140706541-140706591	SK-N-SH	brain:	n/a
4	chr7:140706541-140706591	LNCaP	prostate:	n/a
5	chr7:140714919-140714969	Jurkat	blood:	n/a
6	chr7:140714510-140714560	ProgFib	skin:	n/a
7	chr7:140714661-140714711	Caco-2	colon:	n/a
8	chr7:140714661-140714711	Hela-S3	cervix:	n/a
9	chr7:140706541-140706591	SK-N-SH	brain:	n/a
10	chr7:140706541-140706591	LNCaP	prostate:	n/a
11	chr7:140714919-140714969	Jurkat	blood:	n/a
12	chr7:140714510-140714560	ProgFib	skin:	n/a
13	chr7:140714510-140714560	AG04450	lung:	fetal
14	chr7:140714747-140714797	MCF-7	breast:	n/a
15	chr7:140656922-140656972	MCF-7	breast:	n/a
16	chr7:140714614-140714664	GM12891	blood:	n/a
17	chr7:140714419-140714469	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:140714419-140714469	H1-hESC	embryonic stem cell:	embryo
19	chr7:140715095-140715145	NHBE	bronchial:	n/a
20	chr7:140712089-140712139	GM19239	blood:	n/a
21	chr7:140712089-140712139	AG04449	skin:	fetal
22	chr7:140714412-140714462	AG09319	gingival:	n/a
23	chr7:140657066-140657116	NB4	blood:	n/a
24	chr7:140714661-140714711	HEK293	kidney:	embryo
25	chr7:140714661-140714711	CMK	blood:	n/a
26	chr7:140714419-140714469	T-47D	breast:	n/a
27	chr7:140714814-140714864	HEK293	kidney:	embryo
28	chr7:140715277-140715327	PANC-1	pancreas:	n/a
29	chr7:140714614-140714664	HNPCEpiC	eye:	n/a
30	chr7:140714854-140714904	Caco-2	colon:	n/a
31	chr7:140714588-140714638	GM12891	blood:	n/a
32	chr7:140714670-140714720	PFSK-1	brain:	n/a
33	chr7:140714670-140714720	HCM	heart:	n/a
34	chr7:140712089-140712139	Jurkat	blood:	n/a
35	chr7:140714412-140714462	HepG2	liver:	n/a
36	chr7:140657066-140657116	SK-N-MC	brain:	n/a
37	chr7:140714919-140714969	GM19239	blood:	n/a
38	chr7:140714919-140714969	AG09309	skin:	n/a
39	chr7:140714661-140714711	HEEpiC	esophagus:	n/a
40	chr7:140714781-140714831	AG09309	skin:	n/a
41	chr7:140657066-140657116	HUVEC	blood vessel:	n/a
42	chr7:140706541-140706591	HCF	heart:	n/a
43	chr7:140715095-140715145	AG04450	lung:	fetal
44	chr7:140714412-140714462	ECC-1	luminal epithelium:	n/a
45	chr7:140714412-140714462	HEEpiC	esophagus:	n/a
46	chr7:140714919-140714969	HEK293	kidney:	embryo
47	chr7:140714781-140714831	Caco-2	colon:	n/a
48	chr7:140657066-140657116	ProgFib	skin:	n/a
49	chr7:140714814-140714864	HCM	heart:	n/a
50	chr7:140714919-140714969	T-47D	breast:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:140673174..140674792-chr7:140679004..140681718,2	MCF-7	breast:
2	chr7:140651075..140654377-chr7:140654962..140660080,4	K562	blood:
3	chr7:140667563..140669142-chr7:140674491..140677083,2	MCF-7	breast:
4	chr7:140682579..140684839-chr7:140688833..140690514,2	MCF-7	breast:
5	chr7:140621971..140623569-chr7:140707032..140709391,2	MCF-7	breast:
6	chr7:140696437..140698310-chr7:140712911..140714670,2	K562	blood:
7	chr7:140395386..140400852-chr7:140710628..140716984,11	MCF-7	breast:
8	chr7:140674937..140676218-chr7:140692083..140692979,12	MCF-7	breast:
9	chr7:140661687..140663739-chr7:140664738..140669110,3	MCF-7	breast:
10	chr7:140376267..140379016-chr7:140712794..140714827,3	K562	blood:
11	chr7:140625504..140628313-chr7:140642636..140644756,2	K562	blood:
12	chr7:140623056..140626770-chr7:140716798..140719884,3	K562	blood:
13	chr7:140691421..140693902-chr7:140694734..140697135,2	K562	blood:
14	chr7:140641197..140642073-chr7:140692226..140693040,3	MCF-7	breast:
15	chr7:140705059..140707957-chr7:140712548..140716287,5	K562	blood:
16	chr7:140712784..140717043-chr7:140770770..140775163,8	MCF-7	breast:
17	chr7:140702442..140704379-chr7:140707606..140710163,3	K562	blood:
18	chr7:140681893..140682531-chr7:140692420..140692920,2	MCF-7	breast:
19	chr7:140635874..140638800-chr7:140639576..140642089,2	K562	blood:
20	chr7:140699787..140701784-chr7:140703578..140706034,2	K562	blood:
21	chr7:140672428..140674348-chr7:140681005..140683175,2	K562	blood:
22	chr7:140637228..140638913-chr7:140681368..140684006,2	MCF-7	breast:
23	chr7:140376401..140379049-chr7:140712794..140714370,2	K562	blood:
24	chr7:140689349..140691695-chr7:140694980..140697473,2	MCF-7	breast:
25	chr7:140637553..140639651-chr7:140648268..140650812,2	K562	blood:
26	chr7:140635183..140637575-chr7:140638190..140640935,2	MCF-7	breast:
27	chr7:140654843..140656381-chr7:140659053..140660666,2	K562	blood:
28	chr7:140668526..140670352-chr7:140672310..140674813,2	MCF-7	breast:
29	chr7:140510459..140511610-chr7:140711584..140712563,9	MCF-7	breast:
30	chr7:140675007..140675968-chr7:140692355..140692975,3	MCF-7	breast:
31	chr7:140635183..140637575-chr7:140638190..140640935,2	MCF-7	breast:
32	chr7:140700885..140703018-chr7:140705505..140708464,2	MCF-7	breast:
33	chr7:140700390..140704443-chr7:140712773..140714840,3	K562	blood:
34	chr7:140675000..140676654-chr7:140692083..140692972,8	MCF-7	breast:
35	chr7:140374979..140375913-chr7:140711999..140712535,2	MCF-7	breast:
36	chr7:140510749..140511524-chr7:140683215..140684236,3	K562	blood:
37	chr7:140394719..140399884-chr7:140712014..140716961,9	K562	blood:
38	chr7:140624123..140626561-chr7:140646609..140648992,2	K562	blood:
39	chr7:140688813..140691144-chr7:140711832..140714766,2	K562	blood:
40	chr7:140664931..140667594-chr7:140670729..140673169,2	K562	blood:
41	chr7:140686234..140687769-chr7:140687897..140689543,2	K562	blood:
42	chr7:140706633..140708979-chr7:140709208..140712077,3	MCF-7	breast:
43	chr7:140705945..140708045-chr7:140709551..140711104,2	K562	blood:
44	chr11:67980567..67981241-chr7:140714418..140715202,2	HCT-116	colon:
45	chr7:140672582..140673152-chr7:140692063..140692683,3	MCF-7	breast:
46	chr7:140701510..140704472-chr7:140705422..140707944,2	MCF-7	breast:
47	chr7:140668526..140670352-chr7:140672310..140674813,2	MCF-7	breast:
48	chr7:140701133..140705248-chr7:140712773..140716152,4	K562	blood:
49	chr7:140217421..140218389-chr7:140683292..140684296,3	K562	blood:
50	chr7:140637553..140639651-chr7:140648268..140650812,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS33-2	chr7:140697752-140698690	NONHSAT123700
2	lnc-BRAF-2	chr7:140702410-140704649	ENSG00000273081.1
3	lnc-MRPS33-2	chr7:140698982-140699600	NONHSAT123700

No data

Variant related genes	Relation type
CCT4P1	TF binding region
ENSG00000273081	TF binding region
MRPS33	TF binding region
CCT4P1	CpG island
ENSG00000273081	CpG island
MRPS33	CpG island
ENSG00000110321	chromatin interactions
ENSG00000246308	chromatin interactions
ENSG00000006530	chromatin interactions
ENSG00000090266	chromatin interactions
ENSG00000110066	chromatin interactions
ENSG00000273081	chromatin interactions
ENSG00000211714	chromatin interactions
ENSG00000240889	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000090263	chromatin interactions
ENSG00000263583	chromatin interactions
ENSG00000261115	chromatin interactions
ENSG00000157764	chromatin interactions
ENSG00000242703	chromatin interactions
ENSG00000109046	chromatin interactions
ENSG00000133597	chromatin interactions

Extended variants
information (count: 2312 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536394159	chr7:140637293-140637294	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554851182	chr7:140637306-140637307	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs149099970	chr7:140637351-140637352	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs534199726	chr7:140637409-140637410	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370813152	chr7:140637415-140637416	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs75355403	chr7:140637463-140637464	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576943832	chr7:140637471-140637472	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs192804611	chr7:140637486-140637487	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544203154	chr7:140637497-140637498	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7787206	chr7:140637539-140637540	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs7786103	chr7:140637554-140637555	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs185312684	chr7:140637568-140637569	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs546257462	chr7:140637612-140637613	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187720131	chr7:140637645-140637646	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528308501	chr7:140637671-140637672	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574974445	chr7:140637676-140637677	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200876809	chr7:140637682-140637683	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs35588464	chr7:140637731-140637732	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546540455	chr7:140637738-140637739	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs79848564	chr7:140637794-140637795	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs565183495	chr7:140637862-140637863	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76915274	chr7:140637891-140637892	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs35457739	chr7:140637953-140637954	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs62485383	chr7:140637956-140637957	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs568907761	chr7:140638010-140638011	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs376029406	chr7:140638051-140638052	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2365097	chr7:140638063-140638064	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs548288577	chr7:140638082-140638083	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2365098	chr7:140638083-140638084	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs118028629	chr7:140638085-140638086	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143198496	chr7:140638095-140638096	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192684767	chr7:140638104-140638105	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs183547767	chr7:140638105-140638106	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs118048862	chr7:140638156-140638157	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370979653	chr7:140638248-140638249	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs35374337	chr7:140638313-140638314	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112912892	chr7:140638344-140638345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569888433	chr7:140638373-140638374	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560649090	chr7:140638377-140638378	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs188285200	chr7:140638464-140638465	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs549649260	chr7:140638465-140638466	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565117604	chr7:140638473-140638474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs180967329	chr7:140638520-140638521	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150423391	chr7:140638591-140638592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562441273	chr7:140638601-140638602	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184635703	chr7:140638708-140638709	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189857429	chr7:140638719-140638720	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs181503198	chr7:140638779-140638780	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529887466	chr7:140638879-140638880	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs73497923	chr7:140638895-140638896	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:100)

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
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
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140637400-140638200	Enhancers	Primary B cells from peripheral blood	blood
2	chr7:140653800-140655600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:140656800-140657200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr7:140657200-140669000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:140665200-140665400	Enhancers	Fetal Intestine Small	intestine
6	chr7:140665200-140665400	Enhancers	HepG2	liver
7	chr7:140665200-140667600	Enhancers	Fetal Intestine Large	intestine
8	chr7:140665400-140666400	Weak transcription	Fetal Intestine Small	intestine
9	chr7:140665400-140666400	Weak transcription	HepG2	liver
10	chr7:140666400-140667000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr7:140666400-140667800	Enhancers	Fetal Intestine Small	intestine
12	chr7:140666400-140668800	Enhancers	HepG2	liver
13	chr7:140666800-140667600	Enhancers	Placenta	Placenta
14	chr7:140667600-140672400	Weak transcription	Placenta	Placenta
15	chr7:140667600-140672600	Weak transcription	Fetal Intestine Large	intestine
16	chr7:140667800-140672800	Weak transcription	Fetal Intestine Small	intestine
17	chr7:140668800-140671400	Weak transcription	HepG2	liver
18	chr7:140671400-140672200	Enhancers	HepG2	liver
19	chr7:140672000-140673800	Enhancers	Liver	Liver
20	chr7:140672200-140673600	Flanking Active TSS	HepG2	liver
21	chr7:140672400-140673800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr7:140672400-140673800	Enhancers	Placenta	Placenta
23	chr7:140672400-140674000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:140672600-140673800	Enhancers	Fetal Intestine Large	intestine
25	chr7:140672800-140673800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:140672800-140674000	Enhancers	Adipose Nuclei	Adipose
27	chr7:140672800-140674000	Enhancers	Fetal Intestine Small	intestine
28	chr7:140673000-140673200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr7:140673000-140673600	Enhancers	Hela-S3	cervix
30	chr7:140673000-140674000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr7:140673600-140674200	Enhancers	HepG2	liver
32	chr7:140673800-140675400	Weak transcription	Fetal Intestine Large	intestine
33	chr7:140673800-140675600	Weak transcription	Liver	Liver
34	chr7:140673800-140675600	Weak transcription	Placenta	Placenta
35	chr7:140674000-140675400	Weak transcription	Adipose Nuclei	Adipose
36	chr7:140674000-140675400	Weak transcription	Fetal Intestine Small	intestine
37	chr7:140674000-140675800	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr7:140674200-140674800	Weak transcription	HepG2	liver
39	chr7:140674800-140675400	Enhancers	HepG2	liver
40	chr7:140675400-140676400	Enhancers	Adipose Nuclei	Adipose
41	chr7:140675400-140676400	Flanking Active TSS	HepG2	liver
42	chr7:140675400-140677800	Enhancers	Fetal Intestine Large	intestine
43	chr7:140675400-140677800	Enhancers	Fetal Intestine Small	intestine
44	chr7:140675600-140675800	Enhancers	Liver	Liver
45	chr7:140675600-140676400	Enhancers	Duodenum Mucosa	Duodenum
46	chr7:140675600-140676400	Enhancers	Placenta	Placenta
47	chr7:140675600-140676400	Enhancers	Gastric	stomach
48	chr7:140675600-140676600	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr7:140675600-140676800	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr7:140675800-140676000	Flanking Active TSS	Liver	Liver

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