Variant report

Variant	nsv1027691
Chromosome Location	chr6:74302980-74417450
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2381)
CpG islands
(count:1772)
Chromatin interactive
region (count:164)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:74363545-74364274	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:74365135-74365287	K562	blood:	n/a	n/a
3	ARID3A	chr6:74385173-74385532	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:74318607-74318812	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:74320184-74320573	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:74385213-74385555	K562	blood:	n/a	n/a
7	ARID3A	chr6:74361802-74362994	K562	blood:	n/a	chr6:74362653-74362669
8	ARID3A	chr6:74362319-74362991	HepG2	liver:	n/a	chr6:74362653-74362669
9	ARID3A	chr6:74363690-74364032	K562	blood:	n/a	n/a
10	ARID3A	chr6:74320193-74320518	K562	blood:	n/a	n/a
11	ARID3A	chr6:74354071-74354091	K562	blood:	n/a	n/a
12	ARID3A	chr6:74413930-74414551	HepG2	liver:	n/a	n/a
13	ATF1	chr6:74356261-74356262	K562	blood:	n/a	n/a
14	ATF1	chr6:74414103-74414434	K562	blood:	n/a	n/a
15	ATF2	chr6:74363558-74363988	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:74363804-74364276	GM12878	blood:	n/a	n/a
17	ATF3	chr6:74414085-74414443	K562	blood:	n/a	n/a
18	ATF3	chr6:74405228-74405709	A549	lung:	n/a	n/a
19	ATF3	chr6:74362908-74363139	K562	blood:	n/a	n/a
20	BACH1	chr6:74363514-74363688	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:74405363-74406225	H1-hESC	embryonic stem cell:	n/a	chr6:74405459-74405473
22	BACH1	chr6:74365085-74365103	K562	blood:	n/a	n/a
23	BACH1	chr6:74303331-74303361	K562	blood:	n/a	n/a
24	BACH1	chr6:74362338-74362498	K562	blood:	n/a	n/a
25	BACH1	chr6:74307995-74308040	K562	blood:	n/a	n/a
26	BACH1	chr6:74414474-74414674	K562	blood:	n/a	n/a
27	BATF	chr6:74375738-74375913	GM12878	blood:	n/a	chr6:74375840-74375851 chr6:74375841-74375851
28	BATF	chr6:74405369-74405592	GM12878	blood:	n/a	chr6:74405462-74405473
29	BCL3	chr6:74405337-74405774	GM12878	blood:	n/a	n/a
30	BCL3	chr6:74405115-74405885	A549	lung:	n/a	n/a
31	BCL3	chr6:74363631-74364164	GM12878	blood:	n/a	chr6:74363703-74363716 chr6:74363705-74363714 chr6:74363783-74363792 chr6:74363780-74363793 chr6:74363878-74363891
32	BCL3	chr6:74405240-74405796	A549	lung:	n/a	n/a
33	BCL3	chr6:74363769-74364265	A549	lung:	n/a	chr6:74363783-74363792 chr6:74363780-74363793 chr6:74363878-74363891
34	BCL3	chr6:74401242-74401561	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:74363432-74364249	GM12878	blood:	n/a	chr6:74363460-74363469 chr6:74363703-74363716 chr6:74363705-74363714 chr6:74363783-74363792 chr6:74363780-74363793 chr6:74363878-74363891
36	BCLAF1	chr6:74320128-74320611	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:74364747-74365042	GM12878	blood:	n/a	chr6:74364877-74364898
38	BHLHE40	chr6:74364411-74365419	K562	blood:	n/a	chr6:74364877-74364898
39	BHLHE40	chr6:74385252-74385587	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:74414062-74414305	K562	blood:	n/a	n/a
41	BHLHE40	chr6:74362806-74364143	K562	blood:	n/a	chr6:74363198-74363214 chr6:74363404-74363420 chr6:74363694-74363710
42	BHLHE40	chr6:74363625-74364301	GM12878	blood:	n/a	chr6:74363694-74363710
43	BHLHE40	chr6:74364013-74364213	A549	lung:	n/a	n/a
44	BHLHE40	chr6:74357979-74358200	HepG2	liver:	n/a	n/a
45	BHLHE40	chr6:74405352-74405657	HepG2	liver:	n/a	n/a
46	BHLHE40	chr6:74362437-74362587	K562	blood:	n/a	n/a
47	BHLHE40	chr6:74413977-74414373	HepG2	liver:	n/a	n/a
48	BHLHE40	chr6:74362366-74363307	GM12878	blood:	n/a	chr6:74363198-74363214
49	BHLHE40	chr6:74363535-74364297	HepG2	liver:	n/a	chr6:74363694-74363710
50	BRCA1	chr6:74389993-74390614	Hela-S3	cervix:	n/a	n/a

(count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74363598-74363648	BJ	skin:	n/a
2	chr6:74403105-74403155	LNCaP	prostate:	n/a
3	chr6:74403105-74403155	GM12892	blood:	n/a
4	chr6:74363598-74363648	BJ	skin:	n/a
5	chr6:74403105-74403155	LNCaP	prostate:	n/a
6	chr6:74403105-74403155	GM12892	blood:	n/a
7	chr6:74363018-74363068	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:74363775-74363825	HRPEpiC	eye:	n/a
9	chr6:74363634-74363684	H1-hESC	embryonic stem cell:	embryo
10	chr6:74407227-74407277	K562	blood:	n/a
11	chr6:74363634-74363684	AG09309	skin:	n/a
12	chr6:74363913-74363963	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:74363913-74363963	SK-N-MC	brain:	n/a
14	chr6:74405811-74405861	AG09309	skin:	n/a
15	chr6:74363449-74363499	HMEC	breast:	n/a
16	chr6:74406189-74406239	HEK293	kidney:	embryo
17	chr6:74364149-74364199	HUVEC	blood vessel:	n/a
18	chr6:74403105-74403155	ProgFib	skin:	n/a
19	chr6:74303635-74303685	HRCEpiC	kidney:	n/a
20	chr6:74405811-74405861	HUVEC	blood vessel:	n/a
21	chr6:74363879-74363929	HCM	heart:	n/a
22	chr6:74405447-74405497	HEK293	kidney:	embryo
23	chr6:74404526-74404576	GM12878	blood:	n/a
24	chr6:74363018-74363068	U87	brain:	n/a
25	chr6:74405650-74405700	RPTEC	kidney:	n/a
26	chr6:74405564-74405614	HL-60	blood:	n/a
27	chr6:74405811-74405861	BE2_C	brain:	n/a
28	chr6:74405048-74405098	GM12891	blood:	n/a
29	chr6:74363018-74363068	Caco-2	colon:	n/a
30	chr6:74363913-74363963	NHDF-neo	bronchial:	n/a
31	chr6:74414015-74414065	HCM	heart:	n/a
32	chr6:74405909-74405959	Caco-2	colon:	n/a
33	chr6:74367779-74367829	HCPEpiC	choroid plexus:	n/a
34	chr6:74403105-74403155	HCPEpiC	choroid plexus:	n/a
35	chr6:74403105-74403155	GM19239	blood:	n/a
36	chr6:74363913-74363963	GM12892	blood:	n/a
37	chr6:74405650-74405700	NT2-D1	testis:	n/a
38	chr6:74363634-74363684	LNCaP	prostate:	n/a
39	chr6:74363837-74363887	HIPEpiC	eye:	n/a
40	chr6:74363879-74363929	MCF10A-Er-Src	breast:	n/a
41	chr6:74371222-74371272	BE2_C	brain:	n/a
42	chr6:74363888-74363938	ProgFib	skin:	n/a
43	chr6:74405909-74405959	K562	blood:	n/a
44	chr6:74364700-74364750	AG04449	skin:	fetal
45	chr6:74363913-74363963	BE2_C	brain:	n/a
46	chr6:74404879-74404929	HEK293	kidney:	embryo
47	chr6:74405564-74405614	SK-N-SH_RA	brain:	n/a
48	chr6:74405909-74405959	AG04449	skin:	fetal
49	chr6:74364149-74364199	SKMC	muscle:	n/a
50	chr6:74405811-74405861	HAEpiC	amniotic membrane:	n/a

(count:164 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:74349347..74351323-chr6:74352268..74354035,2	MCF-7	breast:
2	chr19:1591885..1592846-chr6:74363577..74364084,2	Hela-S3	cervix:
3	chr6:74348994..74351945-chr6:74353963..74356232,2	K562	blood:
4	chr6:74405938..74408265-chr6:74438560..74441116,2	MCF-7	breast:
5	chr6:74312525..74315005-chr6:74316974..74319869,2	K562	blood:
6	chr6:74313794..74316156-chr6:74316863..74318391,2	MCF-7	breast:
7	chr6:74353596..74359738-chr6:74361541..74364786,8	MCF-7	breast:
8	chr6:74236818..74238643-chr6:74323624..74325300,2	K562	blood:
9	chr6:74229410..74231742-chr6:74312645..74314509,2	MCF-7	breast:
10	chr6:74363322..74365404-chr6:75950708..75953547,2	MCF-7	breast:
11	chr6:74217534..74219125-chr6:74306574..74309139,2	MCF-7	breast:
12	chr6:74363756..74365330-chr6:74368288..74371193,2	MCF-7	breast:
13	chr6:74312525..74315005-chr6:74316974..74319869,2	K562	blood:
14	chr6:74349101..74350730-chr6:74352362..74353916,2	K562	blood:
15	chr6:74294601..74296941-chr6:74314591..74316170,2	K562	blood:
16	chr6:74310744..74313637-chr6:74316920..74318819,2	MCF-7	breast:
17	chr6:74303250..74306152-chr6:74307378..74309370,2	K562	blood:
18	chr6:74225322..74227120-chr6:74304460..74305982,2	K562	blood:
19	chr6:74207206..74209084-chr6:74351350..74353881,2	K562	blood:
20	chr6:74219718..74234750-chr6:74354945..74369231,56	K562	blood:
21	chr6:74313554..74316552-chr6:74335667..74338657,2	K562	blood:
22	chr6:74230161..74230802-chr6:74362026..74362576,2	Hela-S3	cervix:
23	chr6:74362605..74365737-chr6:74371847..74375318,4	MCF-7	breast:
24	chr6:74321133..74323534-chr6:74341281..74343940,2	K562	blood:
25	chr6:74384825..74386124-chr6:74442444..74443477,21	MCF-7	breast:
26	chr6:74311981..74314645-chr6:74316596..74320386,3	MCF-7	breast:
27	chr6:74236552..74238220-chr6:74320205..74322243,2	MCF-7	breast:
28	chr6:74304294..74306000-chr6:74307805..74310134,2	MCF-7	breast:
29	chr6:74230158..74233335-chr6:74327185..74331083,5	K562	blood:
30	chr6:74289400..74291703-chr6:74315095..74317894,2	K562	blood:
31	chr6:74293523..74296291-chr6:74302711..74304704,2	K562	blood:
32	chr6:74218426..74219208-chr6:74319917..74320421,2	K562	blood:
33	chr6:74320124..74323054-chr6:74351713..74353933,2	MCF-7	breast:
34	chr6:74233458..74235061-chr6:74373728..74376094,2	K562	blood:
35	chr6:74170014..74172890-chr6:74363161..74365164,3	K562	blood:
36	chr6:74346439..74348831-chr6:74363513..74366068,2	K562	blood:
37	chr6:74376095..74378746-chr6:74380712..74383248,2	MCF-7	breast:
38	chr6:74317037..74319356-chr6:74320974..74322634,2	MCF-7	breast:
39	chr6:74228070..74230148-chr6:74344884..74346492,2	K562	blood:
40	chr6:74346702..74349143-chr6:74362515..74365151,2	MCF-7	breast:
41	chr6:74229840..74232671-chr6:74344331..74347609,4	MCF-7	breast:
42	chr6:74313794..74316156-chr6:74316863..74318391,2	MCF-7	breast:
43	chr6:74231875..74233471-chr6:74332835..74334648,2	K562	blood:
44	chr6:74358493..74360158-chr6:74362839..74364793,2	K562	blood:
45	chr6:74404503..74407805-chr6:74409616..74412455,3	MCF-7	breast:
46	chr6:74349347..74351323-chr6:74352268..74354035,2	MCF-7	breast:
47	chr6:74354143..74358709-chr6:74361254..74364709,5	MCF-7	breast:
48	chr6:74224257..74227085-chr6:74333037..74337394,5	K562	blood:
49	chr6:74399537..74401947-chr6:74407305..74409103,2	MCF-7	breast:
50	chr6:74228585..74234219-chr6:74347721..74351601,8	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-1	chr6:74364303-74364586	NONHSAT113578
2	lnc-SLC17A5-1	chr6:74405258-74405298	ENSG00000231652
3	lnc-SLC17A5-1	chr6:74403626-74405298	ENSG00000231652.2
4	lnc-CD109-1	chr6:74364304-74364586	XLOC_005347
5	lnc-CD109-1	chr6:74365811-74366053	NONHSAT113578
6	lnc-SLC17A5-1	chr6:74405555-74405854	ENSG00000231652
7	lnc-CD109-1	chr6:74365848-74365877	XLOC_005347
8	lnc-SLC17A5-1	chr6:74405555-74405854	ENSG00000231652.2
9	lnc-CD109-4	chr6:74328069-74328320	NONHSAT113576

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC17A5	hsa-miR-124-3p	chr6:74304738-74304732
2	SLC17A5	hsa-miR-124-3p	chr6:74304732-74304755

Variant related genes	Relation type
CD109	TF binding region
ENSG00000231652	TF binding region
RPS27P15	TF binding region
SLC17A5	TF binding region
CD109	CpG island
ENSG00000231652	CpG island
RPS27P15	CpG island
SLC17A5	CpG island
ENSG00000071655	chromatin interactions
ENSG00000112695	chromatin interactions
ENSG00000176903	chromatin interactions
ENSG00000119899	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000186812	chromatin interactions
ENSG00000179912	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000203907	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000238464	chromatin interactions
ENSG00000091640	chromatin interactions
ENSG00000156535	chromatin interactions
ENSG00000262429	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000231652	chromatin interactions
ENSG00000223967	chromatin interactions

Extended variants
information (count: 4552 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:4552 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114157122	chr6:74303001-74303002	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs147955223	chr6:74303018-74303019	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs183030233	chr6:74303026-74303027	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573599737	chr6:74303033-74303034	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs540786941	chr6:74303108-74303109	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141885984	chr6:74303170-74303171	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577312148	chr6:74303187-74303188	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs544801600	chr6:74303215-74303216	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs143753884	chr6:74303216-74303217	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543558815	chr6:74303235-74303236	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs530389010	chr6:74303267-74303268	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs143330893	chr6:74303302-74303303	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148144074	chr6:74303308-74303309	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141188189	chr6:74303366-74303367	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs528837086	chr6:74303407-74303408	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs1046716	chr6:74303436-74303437	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs369619857	chr6:74303440-74303441	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559455789	chr6:74303468-74303469	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs547215933	chr6:74303476-74303477	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs199851788	chr6:74303477-74303478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187324549	chr6:74303487-74303488	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539107993	chr6:74303608-74303609	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs9359037	chr6:74303621-74303622	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs116424472	chr6:74303729-74303730	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs569357038	chr6:74303780-74303781	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs150324386	chr6:74303787-74303788	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs191729109	chr6:74303815-74303816	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs670248	chr6:74303829-74303830	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs553278420	chr6:74303886-74303887	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs142349844	chr6:74303891-74303892	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs577447297	chr6:74303898-74303899	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376873526	chr6:74303909-74303910	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182407723	chr6:74303923-74303924	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs145948392	chr6:74303986-74303987	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs575308907	chr6:74303989-74303990	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs542251514	chr6:74303999-74304000	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560914145	chr6:74304000-74304001	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529408804	chr6:74304001-74304002	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs1133168	chr6:74304013-74304014	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566819555	chr6:74304016-74304017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186889797	chr6:74304022-74304023	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs565593896	chr6:74304027-74304028	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs139964473	chr6:74304036-74304037	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs551156682	chr6:74304037-74304038	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs569212197	chr6:74304040-74304041	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547588312	chr6:74304079-74304080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs536793574	chr6:74304112-74304113	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548174264	chr6:74304204-74304205	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540399289	chr6:74304205-74304206	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533473425	chr6:74304212-74304213	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:3018 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74289400-74304000	Weak transcription	Right Ventricle	heart
2	chr6:74289600-74309600	Weak transcription	Lung	lung
3	chr6:74289600-74323800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:74290600-74305800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr6:74290600-74318400	Weak transcription	Small Intestine	intestine
6	chr6:74290600-74338800	Weak transcription	Ovary	ovary
7	chr6:74291000-74307200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:74291000-74315800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:74291000-74323600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:74295200-74303200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:74295200-74321800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:74296000-74317200	Weak transcription	Fetal Brain Female	brain
13	chr6:74296200-74317800	Weak transcription	Colonic Mucosa	Colon
14	chr6:74296200-74317800	Weak transcription	Gastric	stomach
15	chr6:74296200-74322200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:74296200-74322400	Weak transcription	Brain Germinal Matrix	brain
17	chr6:74296200-74332000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr6:74296400-74303200	Weak transcription	Fetal Stomach	stomach
19	chr6:74296400-74307200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr6:74296400-74307200	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr6:74296400-74307400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:74296400-74309000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:74296400-74309000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr6:74296400-74316000	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr6:74296400-74316400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr6:74296400-74318400	Weak transcription	Aorta	Aorta
27	chr6:74296400-74318400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr6:74296400-74325800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr6:74296400-74354800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:74296400-74354800	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr6:74296400-74355000	Weak transcription	Fetal Brain Male	brain
32	chr6:74296600-74303200	Weak transcription	Duodenum Mucosa	Duodenum
33	chr6:74296600-74303600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr6:74296600-74304200	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr6:74296600-74304200	Weak transcription	NHLF	lung
36	chr6:74296600-74307400	Weak transcription	Brain Angular Gyrus	brain
37	chr6:74296600-74307400	Weak transcription	Brain Anterior Caudate	brain
38	chr6:74296600-74308000	Weak transcription	NHEK	skin
39	chr6:74296600-74309000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:74296600-74317600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr6:74296600-74317800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr6:74296600-74319200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr6:74296600-74324000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr6:74296600-74324200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr6:74296600-74324400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr6:74296600-74344000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr6:74296800-74303000	Weak transcription	Osteobl	bone
48	chr6:74296800-74304000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:74296800-74304200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr6:74296800-74307400	Weak transcription	Brain Hippocampus Middle	brain

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