Variant report

Variant	nsv1039002
Chromosome Location	chr10:116643095-116879483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1604)
CpG islands
(count:2016)
Chromatin interactive
region (count:57)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1604 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:116789382-116789792	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:116665348-116665349	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:116697487-116698196	HepG2	liver:	n/a	n/a
4	ATF1	chr10:116697725-116698158	K562	blood:	n/a	n/a
5	ATF1	chr10:116676782-116676906	K562	blood:	n/a	n/a
6	ATF1	chr10:116775074-116775335	K562	blood:	n/a	n/a
7	ATF2	chr10:116697682-116698205	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:116716225-116716691	GM12878	blood:	n/a	n/a
9	ATF2	chr10:116712761-116713172	GM12878	blood:	n/a	n/a
10	ATF2	chr10:116697696-116698258	GM12878	blood:	n/a	n/a
11	ATF2	chr10:116712725-116713282	GM12878	blood:	n/a	n/a
12	ATF2	chr10:116670736-116671263	GM12878	blood:	n/a	n/a
13	ATF2	chr10:116697582-116698196	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr10:116697747-116698104	K562	blood:	n/a	n/a
15	ATF3	chr10:116697789-116698079	HepG2	liver:	n/a	n/a
16	ATF3	chr10:116665174-116665584	HCT-116	colon:	n/a	n/a
17	ATF3	chr10:116697726-116698181	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr10:116697687-116698181	GM12878	blood:	n/a	n/a
19	ATF3	chr10:116697778-116698092	GM12878	blood:	n/a	n/a
20	ATF3	chr10:116697755-116698198	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr10:116697671-116698196	A549	lung:	n/a	n/a
22	ATF3	chr10:116697730-116698169	K562	blood:	n/a	n/a
23	ATF3	chr10:116697701-116698199	A549	lung:	n/a	n/a
24	ATF3	chr10:116697681-116698175	HepG2	liver:	n/a	n/a
25	BACH1	chr10:116678165-116678365	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr10:116852386-116853318	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr10:116853916-116854116	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr10:116685626-116686056	GM12878	blood:	n/a	chr10:116685856-116685867
29	BATF	chr10:116712890-116713128	GM12878	blood:	n/a	chr10:116713021-116713030
30	BATF	chr10:116670818-116671149	GM12878	blood:	n/a	chr10:116671008-116671019
31	BATF	chr10:116685727-116685999	GM12878	blood:	n/a	chr10:116685856-116685867
32	BATF	chr10:116878147-116878431	GM12878	blood:	n/a	chr10:116878279-116878290
33	BATF	chr10:116697782-116698110	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:116694869-116695397	GM12878	blood:	n/a	n/a
35	BCL3	chr10:116697620-116698304	A549	lung:	n/a	n/a
36	BCL3	chr10:116751581-116751840	GM12878	blood:	n/a	n/a
37	BCLAF1	chr10:116697659-116698172	GM12878	blood:	n/a	n/a
38	BCLAF1	chr10:116712754-116713184	GM12878	blood:	n/a	n/a
39	BHLHE40	chr10:116712856-116713181	GM12878	blood:	n/a	n/a
40	BHLHE40	chr10:116789264-116789703	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:116697615-116698384	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:116761761-116762162	GM12878	blood:	n/a	n/a
43	BHLHE40	chr10:116697775-116698294	K562	blood:	n/a	n/a
44	BHLHE40	chr10:116852842-116853079	HepG2	liver:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
45	BHLHE40	chr10:116852859-116853122	GM12878	blood:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
46	BRCA1	chr10:116697849-116698119	HepG2	liver:	n/a	n/a
47	BRCA1	chr10:116697736-116698156	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr10:116697801-116698104	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr10:116699028-116699121	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr10:116697800-116698265	GM12878	blood:	n/a	n/a

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116852687-116852737	HIPEpiC	eye:	n/a
2	chr10:116854028-116854078	HEK293	kidney:	embryo
3	chr10:116654257-116654307	BE2_C	brain:	n/a
4	chr10:116852687-116852737	HIPEpiC	eye:	n/a
5	chr10:116854028-116854078	HEK293	kidney:	embryo
6	chr10:116654257-116654307	BE2_C	brain:	n/a
7	chr10:116852791-116852841	HepG2	liver:	n/a
8	chr10:116852865-116852915	HEK293	kidney:	embryo
9	chr10:116755155-116755205	SK-N-SH	brain:	n/a
10	chr10:116697973-116698023	SKMC	muscle:	n/a
11	chr10:116852811-116852861	IMR90	lung:	fetal
12	chr10:116697604-116697654	SAEC	small airway:	n/a
13	chr10:116854499-116854549	SKMC	muscle:	n/a
14	chr10:116695621-116695671	SAEC	small airway:	n/a
15	chr10:116854499-116854549	U87	brain:	n/a
16	chr10:116852687-116852737	BE2_C	brain:	n/a
17	chr10:116697070-116697120	HRE	kidney:	n/a
18	chr10:116697973-116698023	BE2_C	brain:	n/a
19	chr10:116654257-116654307	AG09319	gingival:	n/a
20	chr10:116701397-116701447	GM12891	blood:	n/a
21	chr10:116697924-116697974	PANC-1	pancreas:	n/a
22	chr10:116698168-116698218	Caco-2	colon:	n/a
23	chr10:116697907-116697957	NB4	blood:	n/a
24	chr10:116701397-116701447	BE2_C	brain:	n/a
25	chr10:116697604-116697654	HPAEpiC	pulmonary alveolar:	n/a
26	chr10:116852470-116852520	ProgFib	skin:	n/a
27	chr10:116698451-116698501	HUVEC	blood vessel:	n/a
28	chr10:116854499-116854549	AG09309	skin:	n/a
29	chr10:116698331-116698381	ovcar-3	ovarian:	n/a
30	chr10:116697924-116697974	SK-N-SH_RA	brain:	n/a
31	chr10:116852470-116852520	HMEC	breast:	n/a
32	chr10:116852865-116852915	SK-N-MC	brain:	n/a
33	chr10:116659330-116659380	U87	brain:	n/a
34	chr10:116697985-116698035	H1-hESC	embryonic stem cell:	embryo
35	chr10:116697604-116697654	NHBE	bronchial:	n/a
36	chr10:116659330-116659380	AG04450	lung:	fetal
37	chr10:116701397-116701447	IMR90	lung:	fetal
38	chr10:116697985-116698035	A549	lung:	n/a
39	chr10:116697985-116698035	T-47D	breast:	n/a
40	chr10:116849473-116849523	Hepatocyte	liver:	n/a
41	chr10:116852791-116852841	NH-A	brain:	n/a
42	chr10:116697907-116697957	GM12878	blood:	n/a
43	chr10:116755155-116755205	MCF-7	breast:	n/a
44	chr10:116852811-116852861	Jurkat	blood:	n/a
45	chr10:116852811-116852861	SK-N-MC	brain:	n/a
46	chr10:116852811-116852861	HEEpiC	esophagus:	n/a
47	chr10:116697907-116697957	HNPCEpiC	eye:	n/a
48	chr10:116852865-116852915	A549	lung:	n/a
49	chr10:116853664-116853714	ovcar-3	ovarian:	n/a
50	chr10:116823300-116823350	GM06990	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:116747111..116749787-chr10:116750033..116752654,2	MCF-7	breast:
2	chr10:116702780..116705298-chr10:116717545..116719063,2	MCF-7	breast:
3	chr10:116653223..116654731-chr10:116697488..116699570,2	MCF-7	breast:
4	chr10:116681770..116684136-chr10:116685910..116687423,2	MCF-7	breast:
5	chr10:116697944..116699780-chr10:116701947..116704062,3	MCF-7	breast:
6	chr10:116639834..116644233-chr10:116697414..116700996,4	MCF-7	breast:
7	chr10:116702154..116704292-chr10:116706734..116708655,2	K562	blood:
8	chr10:116650665..116651165-chr8:43092430..43093407,2	MCF-7	breast:
9	chr10:116777335..116780032-chr10:116781033..116782789,3	MCF-7	breast:
10	chr10:116704116..116706945-chr10:116736952..116739415,3	K562	blood:
11	chr10:116691563..116693571-chr10:116695644..116697264,2	MCF-7	breast:
12	chr10:116668856..116672009-chr10:116672893..116675260,3	K562	blood:
13	chr10:116782925..116784506-chr10:116795352..116797997,2	MCF-7	breast:
14	chr10:116718109..116720528-chr10:116722759..116724977,2	K562	blood:
15	chr10:116681770..116684136-chr10:116685910..116687423,2	MCF-7	breast:
16	chr10:116697901..116698524-chr14:74485364..74486290,2	NB4	blood:
17	chr10:116697085..116699595-chr10:116722929..116725734,2	MCF-7	breast:
18	chr10:116747111..116749787-chr10:116750033..116752654,2	MCF-7	breast:
19	chr10:116695542..116700856-chr10:116705111..116709890,7	MCF-7	breast:
20	chr10:116696953..116700606-chr10:116852065..116855116,4	MCF-7	breast:
21	chr10:116698018..116699998-chr10:116702576..116705255,2	K562	blood:
22	chr10:116708122..116710473-chr10:116713973..116715764,2	MCF-7	breast:
23	chr10:116818326..116821419-chr10:116821811..116825642,4	K562	blood:
24	chr10:116751496..116754432-chr10:116766030..116768303,2	MCF-7	breast:
25	chr10:116696953..116700606-chr10:116852065..116855116,4	MCF-7	breast:
26	chr10:116260065..116262593-chr10:116698525..116701420,2	MCF-7	breast:
27	chr10:116731834..116734462-chr10:116737301..116739152,2	K562	blood:
28	chr10:116818326..116821419-chr10:116821811..116825642,4	K562	blood:
29	chr10:116696802..116699955-chr10:116713362..116716908,4	MCF-7	breast:
30	chr10:116697582..116698356-chr11:94964692..94965293,2	NB4	blood:
31	chr10:116721231..116723812-chr10:116727155..116729844,2	K562	blood:
32	chr10:116682984..116685830-chr10:116689938..116692838,2	K562	blood:
33	chr10:116682984..116685830-chr10:116689938..116692838,2	K562	blood:
34	chr10:116666525..116669510-chr10:116698929..116700670,2	MCF-7	breast:
35	chr10:116708122..116710473-chr10:116713973..116715764,2	MCF-7	breast:
36	chr10:116704116..116706945-chr10:116736952..116739415,3	K562	blood:
37	chr10:116668856..116672009-chr10:116672893..116675260,3	K562	blood:
38	chr10:116739587..116740088-chr8:43092410..43093248,2	MCF-7	breast:
39	chr10:116702154..116704292-chr10:116706734..116708655,2	K562	blood:
40	chr10:116697261..116699951-chr10:116709059..116711441,4	MCF-7	breast:
41	chr10:116777335..116780032-chr10:116781033..116782789,3	MCF-7	breast:
42	chr10:116722299..116723812-chr10:116727808..116729844,2	K562	blood:
43	chr10:116702780..116705298-chr10:116717545..116719063,2	MCF-7	breast:
44	chr10:116734818..116737513-chr10:116740129..116742144,2	MCF-7	breast:
45	chr10:116869478..116872129-chr10:116874892..116876661,2	MCF-7	breast:
46	chr10:116697590..116699653-chr10:116710525..116713221,2	MCF-7	breast:
47	chr10:116869478..116872129-chr10:116874892..116876661,2	MCF-7	breast:
48	chr10:116731834..116734462-chr10:116737301..116739152,2	K562	blood:
49	chr10:116691563..116693571-chr10:116695644..116697264,2	MCF-7	breast:
50	chr10:116718109..116720528-chr10:116722759..116724977,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRUB1-2	chr10:116745192-116745287	NONHSAT016469
2	lnc-TRUB1-1	chr10:116756233-116756352	NONHSAT016471
3	lnc-TRUB1-1	chr10:116755202-116755297	XLOC_008629
4	lnc-TRUB1-1	chr10:116754416-116754544	XLOC_008629
5	lnc-TRUB1-1	chr10:116754301-116754688	NONHSAT016471
6	lnc-TRUB1-3	chr10:116751678-116751759	NONHSAT016470
7	lnc-TRUB1-2	chr10:116744406-116744534	NONHSAT016469
8	lnc-TRUB1-2	chr10:116746224-116746342	NONHSAT016469
9	lnc-TRUB1-1	chr10:116756234-116756352	XLOC_008629
10	lnc-ABLIM1-4	chr10:116786294-116786531	NONHSAT016473
11	lnc-TRUB1-3	chr10:116751175-116751631	NONHSAT016470
12	lnc-TRUB1-3	chr10:116751805-116751835	NONHSAT016470
13	lnc-ABLIM1-4	chr10:116787612-116787799	NONHSAT016473
14	lnc-TRUB1-1	chr10:116755201-116755297	NONHSAT016471

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TRUB1	hsa-miR-17-5p	chr10:116735871-116735894

Variant related genes	Relation type
ATRNL1	TF binding region
TRUB1	TF binding region
ENSG00000226428	TF binding region
RNU6-1121P	TF binding region
ENSG00000236799	TF binding region
ATRNL1	CpG island
TRUB1	CpG island
ENSG00000226428	CpG island
RNU6-1121P	CpG island
ENSG00000236799	CpG island
ENSG00000107518	chromatin interactions
ENSG00000236799	chromatin interactions
ENSG00000165832	chromatin interactions
ENSG00000245552	chromatin interactions
ENSG00000187097	chromatin interactions
ENSG00000252611	chromatin interactions
ENSG00000137100	chromatin interactions
ENSG00000119636	chromatin interactions
ENSG00000229668	chromatin interactions

Extended variants
information (count: 8342 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:8342 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17794346	chr10:116643095-116643096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376209169	chr10:116643101-116643102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs531748538	chr10:116643102-116643103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372512782	chr10:116643109-116643110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs193275293	chr10:116643110-116643111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367596632	chr10:116643139-116643140	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140513786	chr10:116643208-116643209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs532438532	chr10:116643239-116643240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs371738610	chr10:116643241-116643242	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183706415	chr10:116643277-116643278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs565650838	chr10:116643297-116643298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529728247	chr10:116643403-116643404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547910350	chr10:116643404-116643405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs113880401	chr10:116643426-116643427	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556705398	chr10:116643429-116643430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188421378	chr10:116643432-116643433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375730672	chr10:116643494-116643495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145574506	chr10:116643545-116643546	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369478249	chr10:116643559-116643560	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572076305	chr10:116643596-116643597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531958646	chr10:116643601-116643602	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542598524	chr10:116643614-116643615	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372883073	chr10:116643615-116643616	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs533708725	chr10:116643621-116643622	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576479105	chr10:116643635-116643636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs543594459	chr10:116643638-116643639	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560459687	chr10:116643757-116643758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs79415956	chr10:116643842-116643843	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs10885622	chr10:116643844-116643845	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs541297766	chr10:116643902-116643903	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191754042	chr10:116643914-116643915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs78736910	chr10:116643956-116643957	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs184341733	chr10:116643958-116643959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527865753	chr10:116643997-116643998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs548163302	chr10:116644069-116644070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374117400	chr10:116644090-116644091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569589145	chr10:116644094-116644095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs527514172	chr10:116644124-116644125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs17721283	chr10:116644141-116644142	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs571482005	chr10:116644159-116644160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs145566574	chr10:116644175-116644176	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553982023	chr10:116644182-116644183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs74158087	chr10:116644286-116644287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs373326904	chr10:116644315-116644316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs7898347	chr10:116644324-116644325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs189864407	chr10:116644349-116644350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576368809	chr10:116644397-116644398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543870819	chr10:116644398-116644399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181509700	chr10:116644404-116644405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577448135	chr10:116644407-116644408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3062 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116641600-116645400	Weak transcription	Stomach Mucosa	stomach
2	chr10:116642000-116643200	Enhancers	Colon Smooth Muscle	Colon
3	chr10:116642000-116643200	Enhancers	Hela-S3	cervix
4	chr10:116642200-116643200	Enhancers	HMEC	breast
5	chr10:116642200-116655800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr10:116642600-116643200	Enhancers	A549	lung
7	chr10:116645400-116645600	Enhancers	Stomach Mucosa	stomach
8	chr10:116645400-116645800	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr10:116655400-116655800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr10:116655600-116656800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr10:116655800-116656200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr10:116655800-116657200	Enhancers	H1 Cell Line	embryonic stem cell
13	chr10:116655800-116657200	Enhancers	HMEC	breast
14	chr10:116656000-116656600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr10:116656000-116656600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr10:116656000-116656800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr10:116656000-116657200	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr10:116656000-116657200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:116656200-116657200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:116656200-116657200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:116656400-116656600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr10:116656400-116657200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr10:116656400-116657200	Enhancers	NHEK	skin
24	chr10:116656600-116660400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:116657800-116658000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr10:116658200-116661400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr10:116660400-116660800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:116660600-116660800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:116660800-116666200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr10:116660800-116666400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:116660800-116676400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:116661400-116661800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr10:116661400-116662000	Enhancers	A549	lung
34	chr10:116661400-116662400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr10:116661400-116662400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr10:116661600-116662400	Enhancers	HSMMtube	muscle
37	chr10:116661600-116662400	Enhancers	Osteobl	bone
38	chr10:116661600-116662600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr10:116661800-116662000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:116661800-116662200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr10:116661800-116662400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr10:116661800-116662400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr10:116661800-116662400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:116661800-116662400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr10:116661800-116662400	Enhancers	HSMM	muscle
46	chr10:116661800-116662400	Enhancers	NH-A	brain
47	chr10:116662000-116662200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr10:116662000-116664200	Weak transcription	A549	lung
49	chr10:116662200-116662400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr10:116662200-116666200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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