Variant report

Variant	nsv1034448
Chromosome Location	chr6:118698169-119016383
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3113)
CpG islands
(count:2260)
Chromatin interactive
region (count:168)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3113 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:118972660-118972662	K562	blood:	n/a	n/a
2	ARID3A	chr6:118952118-118952318	K562	blood:	n/a	n/a
3	ARID3A	chr6:118872218-118872638	K562	blood:	n/a	n/a
4	ARID3A	chr6:118981514-118981884	K562	blood:	n/a	n/a
5	ARID3A	chr6:118980569-118981224	K562	blood:	n/a	n/a
6	ARID3A	chr6:118827198-118827857	K562	blood:	n/a	n/a
7	ARID3A	chr6:118962153-118962414	K562	blood:	n/a	n/a
8	ARID3A	chr6:118789925-118790949	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:118872268-118872562	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:118858668-118859424	K562	blood:	n/a	n/a
11	ARID3A	chr6:118830184-118830599	K562	blood:	n/a	n/a
12	ARID3A	chr6:118823438-118823630	K562	blood:	n/a	n/a
13	ARID3A	chr6:118902902-118903335	K562	blood:	n/a	n/a
14	ATF1	chr6:118981295-118981858	K562	blood:	n/a	n/a
15	ATF1	chr6:118989980-118990521	K562	blood:	n/a	n/a
16	ATF1	chr6:118998340-118998673	K562	blood:	n/a	n/a
17	ATF1	chr6:118857664-118857956	K562	blood:	n/a	n/a
18	ATF1	chr6:118858821-118859136	K562	blood:	n/a	n/a
19	ATF1	chr6:118902847-118903468	K562	blood:	n/a	n/a
20	ATF2	chr6:118844367-118844780	GM12878	blood:	n/a	n/a
21	ATF2	chr6:118788378-118788709	GM12878	blood:	n/a	n/a
22	ATF3	chr6:118858885-118859169	K562	blood:	n/a	n/a
23	ATF3	chr6:118790642-118790921	K562	blood:	n/a	n/a
24	ATF3	chr6:118827141-118827527	K562	blood:	n/a	n/a
25	ATF3	chr6:118902749-118903214	K562	blood:	n/a	n/a
26	BACH1	chr6:118971853-118972007	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:118708234-118708493	K562	blood:	n/a	n/a
28	BACH1	chr6:118721799-118722067	K562	blood:	n/a	n/a
29	BACH1	chr6:118721836-118722106	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:118972261-118972660	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:119002377-119002398	K562	blood:	n/a	n/a
32	BACH1	chr6:118972890-118973479	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:118708219-118708390	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr6:118806716-118807107	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
35	BATF	chr6:118806735-118807083	GM12878	blood:	n/a	chr6:118806904-118806914 chr6:118806903-118806914
36	BATF	chr6:118844430-118844743	GM12878	blood:	n/a	n/a
37	BATF	chr6:118844451-118844653	GM12878	blood:	n/a	n/a
38	BCLAF1	chr6:118960390-118960806	GM12878	blood:	n/a	chr6:118960673-118960682
39	BCLAF1	chr6:118971615-118972203	GM12878	blood:	n/a	chr6:118971948-118971961 chr6:118971739-118971752 chr6:118971950-118971959 chr6:118972114-118972127
40	BHLHE40	chr6:118971677-118973245	GM12878	blood:	n/a	chr6:118971942-118971958
41	BHLHE40	chr6:118972034-118973184	K562	blood:	n/a	n/a
42	BHLHE40	chr6:118826979-118827557	K562	blood:	n/a	n/a
43	BHLHE40	chr6:118875834-118875898	GM12878	blood:	n/a	n/a
44	BHLHE40	chr6:118981332-118981743	K562	blood:	n/a	n/a
45	BHLHE40	chr6:118858863-118859144	K562	blood:	n/a	n/a
46	BHLHE40	chr6:118790184-118790852	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:118902939-118903073	K562	blood:	n/a	n/a
48	BHLHE40	chr6:118806741-118807388	GM12878	blood:	n/a	n/a
49	BRCA1	chr6:118972160-118972360	GM12878	blood:	n/a	n/a
50	BRCA1	chr6:118971487-118971792	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:118976630-118976680	GM12891	blood:	n/a
2	chr6:118973597-118973647	HRPEpiC	eye:	n/a
3	chr6:118973309-118973359	BJ	skin:	n/a
4	chr6:118976630-118976680	GM12891	blood:	n/a
5	chr6:118973597-118973647	HRPEpiC	eye:	n/a
6	chr6:118973309-118973359	BJ	skin:	n/a
7	chr6:118972731-118972781	HL-60	blood:	n/a
8	chr6:118973309-118973359	U87	brain:	n/a
9	chr6:118709682-118709732	GM12878	blood:	n/a
10	chr6:118973309-118973359	CMK	blood:	n/a
11	chr6:118822131-118822181	HepG2	liver:	n/a
12	chr6:118973597-118973647	K562	blood:	n/a
13	chr6:118822131-118822181	HCM	heart:	n/a
14	chr6:118973695-118973745	PFSK-1	brain:	n/a
15	chr6:118973337-118973387	NHBE	bronchial:	n/a
16	chr6:118973695-118973745	HAEpiC	amniotic membrane:	n/a
17	chr6:118989666-118989716	PFSK-1	brain:	n/a
18	chr6:118873071-118873121	HCPEpiC	choroid plexus:	n/a
19	chr6:118909918-118909968	PrEC	prostate:	n/a
20	chr6:119009025-119009075	ovcar-3	ovarian:	n/a
21	chr6:118822466-118822516	NH-A	brain:	n/a
22	chr6:118972232-118972282	HCF	heart:	n/a
23	chr6:118822505-118822555	HepG2	liver:	n/a
24	chr6:118822466-118822516	SK-N-MC	brain:	n/a
25	chr6:118972834-118972884	HCT-116	colon:	n/a
26	chr6:118822131-118822181	HIPEpiC	eye:	n/a
27	chr6:118823964-118824014	NB4	blood:	n/a
28	chr6:118909918-118909968	HRCEpiC	kidney:	n/a
29	chr6:118909918-118909968	SK-N-SH_RA	brain:	n/a
30	chr6:118823964-118824014	GM12878	blood:	n/a
31	chr6:118973597-118973647	NH-A	brain:	n/a
32	chr6:118821449-118821499	HCM	heart:	n/a
33	chr6:118823964-118824014	HL-60	blood:	n/a
34	chr6:118971624-118971674	PFSK-1	brain:	n/a
35	chr6:118973057-118973107	MCF10A-Er-Src	breast:	n/a
36	chr6:118973021-118973071	HepG2	liver:	n/a
37	chr6:118971624-118971674	IMR90	lung:	fetal
38	chr6:118973695-118973745	A549	lung:	n/a
39	chr6:118822505-118822555	ProgFib	skin:	n/a
40	chr6:118973046-118973096	AG04449	skin:	fetal
41	chr6:118973046-118973096	HIPEpiC	eye:	n/a
42	chr6:118909918-118909968	AG09309	skin:	n/a
43	chr6:118709682-118709732	LNCaP	prostate:	n/a
44	chr6:118989666-118989716	Jurkat	blood:	n/a
45	chr6:118903047-118903097	NB4	blood:	n/a
46	chr6:118873071-118873121	GM12891	blood:	n/a
47	chr6:118972232-118972282	AG04450	lung:	fetal
48	chr6:118973353-118973403	Jurkat	blood:	n/a
49	chr6:118973309-118973359	Jurkat	blood:	n/a
50	chr6:118989666-118989716	HCT-116	colon:	n/a

(count:168 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:118962546..118964256-chr6:118970270..118972608,2	MCF-7	breast:
2	chr6:118988812..118990874-chr6:118994587..118996786,2	K562	blood:
3	chr6:118780254..118782532-chr6:118784311..118786447,2	K562	blood:
4	chr6:118604657..118606544-chr6:118829791..118831020,17	MCF-7	breast:
5	chr6:118901771..118902663-chr6:118939336..118940142,2	MCF-7	breast:
6	chr6:118729437..118730312-chr6:118828228..118829001,2	MCF-7	breast:
7	chr22:44769853..44770735-chr6:118990487..118991265,2	MCF-7	breast:
8	chr6:118905497..118907408-chr6:118920434..118922584,2	MCF-7	breast:
9	chr6:118840065..118842365-chr6:118844866..118846753,2	K562	blood:
10	chr6:118864850..118867367-chr6:118869435..118872400,3	K562	blood:
11	chr6:118985710..118987649-chr6:118989150..118991916,2	K562	blood:
12	chr6:118787172..118789058-chr6:118799160..118802134,2	MCF-7	breast:
13	chr6:118973033..118976583-chr6:118976702..118979971,3	MCF-7	breast:
14	chr6:118954415..118957401-chr6:118960640..118962641,2	K562	blood:
15	chr6:119012354..119023494-chr6:119027532..119033557,15	K562	blood:
16	chr6:118985710..118987649-chr6:118989150..118991916,2	K562	blood:
17	chr6:26157794..26158411-chr6:118872084..118872729,2	Hela-S3	cervix:
18	chr6:118829745..118830555-chr6:118939535..118940562,3	MCF-7	breast:
19	chr6:118966044..118969834-chr6:118971302..118974528,3	MCF-7	breast:
20	chr6:118904992..118906769-chr6:118911798..118913506,2	MCF-7	breast:
21	chr6:118911659..118913599-chr6:118915475..118918005,2	K562	blood:
22	chr6:118985895..118989345-chr6:119015029..119017625,3	K562	blood:
23	chr6:118830553..118833373-chr6:118834538..118836187,2	K562	blood:
24	chr6:118807029..118809570-chr6:118811844..118815669,3	K562	blood:
25	chr6:118836380..118838045-chr6:118841416..118842970,2	K562	blood:
26	chr6:118785090..118787598-chr6:118788588..118791093,3	K562	blood:
27	chr6:118958389..118960961-chr6:118962868..118964919,2	K562	blood:
28	chr6:118829745..118830555-chr6:118939535..118940562,3	MCF-7	breast:
29	chr6:118886433..118887071-chr6:119121474..119122076,2	MCF-7	breast:
30	chr6:118830553..118833464-chr6:118833711..118836187,2	K562	blood:
31	chr6:118953209..118955124-chr6:118961849..118964677,2	K562	blood:
32	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
33	chr6:118807810..118810020-chr6:118811825..118813344,2	K562	blood:
34	chr6:118858794..118860547-chr6:118861810..118864378,3	K562	blood:
35	chr6:118977517..118980348-chr6:118986192..118988530,2	K562	blood:
36	chr6:119004382..119006834-chr6:119024515..119026911,2	K562	blood:
37	chr6:118911659..118913599-chr6:118915475..118918005,2	K562	blood:
38	chr6:118845234..118848026-chr6:118887537..118889460,2	K562	blood:
39	chr6:118797594..118799964-chr6:118802323..118804468,2	K562	blood:
40	chr6:118793164..118795784-chr6:118796166..118797869,2	MCF-7	breast:
41	chr6:118605730..118606559-chr6:118871514..118872878,6	MCF-7	breast:
42	chr6:118987546..118990459-chr6:118992070..118994560,4	K562	blood:
43	chr6:118870709..118872352-chr6:118873999..118876158,2	K562	blood:
44	chr6:119002292..119005255-chr6:119017824..119020721,2	K562	blood:
45	chr6:118886432..118887044-chr6:118901651..118902441,2	MCF-7	breast:
46	chr6:118604766..118605648-chr6:118871523..118872923,8	MCF-7	breast:
47	chr6:118891495..118893998-chr6:118896946..118899514,2	K562	blood:
48	chr6:118963482..118965586-chr6:118971690..118974055,2	MCF-7	breast:
49	chr6:118953624..118955597-chr6:118963177..118965168,2	K562	blood:
50	chr6:119000908..119005300-chr6:119005318..119008717,6	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MCM9-2	chr6:118977926-118978284	NONHSAT114697
2	lnc-PLN-2	chr6:118772307-118773627	NONHSAT114692
3	lnc-MCM9-2	chr6:118985574-118985684	NONHSAT114697
4	lnc-PLN-1	chr6:118822536-118824996	NR_002730

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C6orf204	hsa-miR-335-5p	chr6:118812647-118812669

Variant related genes	Relation type
ENSG00000216809	TF binding region
BRD7P3	TF binding region
SSXP10	TF binding region
PLN	TF binding region
CEP85L	TF binding region
ENSG00000216809	CpG island
BRD7P3	CpG island
SSXP10	CpG island
PLN	CpG island
CEP85L	CpG island
ENSG00000253194	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000216809	chromatin interactions
ENSG00000111860	chromatin interactions
ENSG00000198523	chromatin interactions
ENSG00000111877	chromatin interactions
ENSG00000158373	chromatin interactions

Extended variants
information (count: 11517 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:11517 , 50 per page) page: 1 2 3 4 5 6 7 ... 231

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6569017	chr6:118698169-118698170	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72967578	chr6:118698179-118698180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568242027	chr6:118698234-118698235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75508915	chr6:118698237-118698238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542680149	chr6:118698302-118698303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562414129	chr6:118698345-118698346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557969317	chr6:118698380-118698381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569955008	chr6:118698437-118698438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531436904	chr6:118698440-118698441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs116303398	chr6:118698478-118698479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs397968105	chr6:118698508-118698509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9320650	chr6:118698509-118698510	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs527529378	chr6:118698600-118698601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547265868	chr6:118698639-118698640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367816923	chr6:118698655-118698656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567256803	chr6:118698662-118698663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148258766	chr6:118698680-118698681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182656613	chr6:118698690-118698691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557127615	chr6:118698730-118698731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556543932	chr6:118698769-118698770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371227792	chr6:118698787-118698788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570007085	chr6:118698844-118698845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79403049	chr6:118698850-118698851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558825449	chr6:118698875-118698876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572600463	chr6:118698949-118698950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75363923	chr6:118698980-118698981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186533997	chr6:118699001-118699002	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575227774	chr6:118699004-118699005	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542596194	chr6:118699009-118699010	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373839505	chr6:118699049-118699050	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13192975	chr6:118699070-118699071	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs146342159	chr6:118699071-118699072	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191444597	chr6:118699131-118699132	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183290568	chr6:118699170-118699171	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543054900	chr6:118699185-118699186	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564857484	chr6:118699249-118699250	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs578028450	chr6:118699263-118699264	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547204309	chr6:118699265-118699266	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71559827	chr6:118699267-118699268	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539917068	chr6:118699283-118699284	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561674387	chr6:118699325-118699326	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560820683	chr6:118699328-118699329	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72967581	chr6:118699329-118699330	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs72967582	chr6:118699332-118699333	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6928210	chr6:118699394-118699395	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538705700	chr6:118699401-118699402	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs552621937	chr6:118699438-118699439	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs566215807	chr6:118699461-118699462	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs535198343	chr6:118699531-118699532	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs188735971	chr6:118699541-118699542	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	22522925	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Pancreatic cancer	17952125	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:5457 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118688200-118700200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:118691400-118700400	Enhancers	Fetal Heart	heart
3	chr6:118692200-118699000	Weak transcription	Psoas Muscle	Psoas
4	chr6:118694200-118699600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr6:118694800-118698200	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr6:118696000-118698200	Weak transcription	Left Ventricle	heart
7	chr6:118696200-118698200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:118696200-118699000	Weak transcription	Right Atrium	heart
9	chr6:118698200-118698400	Enhancers	Left Ventricle	heart
10	chr6:118698200-118698400	Enhancers	Skeletal Muscle Male	skeletal muscle
11	chr6:118698200-118699000	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr6:118698200-118699600	Enhancers	Fetal Thymus	thymus
13	chr6:118698200-118699800	Enhancers	Thymus	Thymus
14	chr6:118698400-118698800	Weak transcription	Left Ventricle	heart
15	chr6:118698400-118698800	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr6:118698600-118698800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:118698800-118699000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:118698800-118699000	Enhancers	Left Ventricle	heart
19	chr6:118698800-118699000	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr6:118698800-118699800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:118698800-118700400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr6:118699000-118699200	Flanking Active TSS	Left Ventricle	heart
23	chr6:118699000-118699400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr6:118699000-118699400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:118699000-118699400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:118699000-118699400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
27	chr6:118699000-118699400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr6:118699000-118699600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr6:118699000-118699600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:118699000-118699600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:118699000-118699600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:118699000-118699600	Enhancers	Fetal Muscle Trunk	muscle
33	chr6:118699000-118699600	Enhancers	Fetal Muscle Leg	muscle
34	chr6:118699000-118699600	Enhancers	Psoas Muscle	Psoas
35	chr6:118699000-118699600	Enhancers	Right Atrium	heart
36	chr6:118699000-118699800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:118699000-118699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:118699000-118700000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr6:118699200-118699400	Enhancers	Left Ventricle	heart
40	chr6:118699400-118699600	Active TSS	Left Ventricle	heart
41	chr6:118699400-118699600	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr6:118699400-118699800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:118699600-118700400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr6:118699600-118707600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:118699600-118716400	Weak transcription	Psoas Muscle	Psoas
46	chr6:118700200-118700400	Enhancers	Rectal Smooth Muscle	rectum
47	chr6:118700200-118700800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:118700800-118708800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:118702200-118702400	Weak transcription	Rectal Smooth Muscle	rectum
50	chr6:118702400-118703000	Enhancers	Stomach Smooth Muscle	stomach

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