Variant report

Variant	nsv884103
Chromosome Location	chr6:30729487-30755668
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1564)
CpG islands
(count:489)
Chromatin interactive
region (count:78)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1564 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:30749425-30750806	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:30753786-30754521	K562	blood:	n/a	n/a
3	ARID3A	chr6:30736903-30737815	K562	blood:	n/a	n/a
4	ARID3A	chr6:30731119-30732417	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:30732117-30732331	K562	blood:	n/a	n/a
6	ARID3A	chr6:30736577-30737865	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:30749571-30750337	K562	blood:	n/a	n/a
8	ATF1	chr6:30753726-30753910	K562	blood:	n/a	n/a
9	ATF1	chr6:30749451-30750290	K562	blood:	n/a	chr6:30749808-30749822
10	ATF1	chr6:30737082-30737729	K562	blood:	n/a	n/a
11	ATF1	chr6:30732026-30732337	K562	blood:	n/a	n/a
12	ATF1	chr6:30735190-30735588	K562	blood:	n/a	n/a
13	ATF2	chr6:30734954-30735856	GM12878	blood:	n/a	n/a
14	ATF2	chr6:30749323-30750278	GM12878	blood:	n/a	chr6:30749808-30749822
15	ATF2	chr6:30737340-30737709	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:30749467-30750091	GM12878	blood:	n/a	chr6:30749808-30749822
17	ATF2	chr6:30734968-30735793	GM12878	blood:	n/a	n/a
18	ATF3	chr6:30736926-30737865	A549	lung:	n/a	chr6:30737123-30737132
19	ATF3	chr6:30736826-30737754	K562	blood:	n/a	chr6:30737123-30737132
20	ATF3	chr6:30749273-30750308	K562	blood:	n/a	n/a
21	ATF3	chr6:30749384-30750697	A549	lung:	n/a	n/a
22	ATF3	chr6:30753677-30753978	K562	blood:	n/a	n/a
23	ATF3	chr6:30749499-30749934	K562	blood:	n/a	n/a
24	ATF3	chr6:30737100-30737691	K562	blood:	n/a	chr6:30737123-30737132
25	ATF3	chr6:30749244-30750106	A549	lung:	n/a	n/a
26	ATF3	chr6:30737226-30737823	A549	lung:	n/a	n/a
27	BACH1	chr6:30737604-30737631	K562	blood:	n/a	n/a
28	BACH1	chr6:30753717-30754453	K562	blood:	n/a	n/a
29	BACH1	chr6:30737510-30737657	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:30753854-30753986	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr6:30749650-30749929	GM12878	blood:	n/a	n/a
32	BATF	chr6:30735033-30735742	GM12878	blood:	n/a	n/a
33	BATF	chr6:30737375-30737613	GM12878	blood:	n/a	chr6:30737512-30737523
34	BATF	chr6:30735027-30735618	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:30735061-30735393	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:30737123-30737391	GM12878	blood:	n/a	chr6:30737225-30737234 chr6:30737222-30737231
37	BCL11A	chr6:30735428-30735752	GM12878	blood:	n/a	n/a
38	BCL11A	chr6:30735105-30735759	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:30737072-30737365	GM12878	blood:	n/a	chr6:30737225-30737234 chr6:30737222-30737231
40	BCL3	chr6:30749469-30750912	A549	lung:	n/a	chr6:30749933-30749942
41	BCL3	chr6:30754688-30754948	GM12878	blood:	n/a	n/a
42	BCL3	chr6:30736667-30737950	A549	lung:	n/a	chr6:30736998-30737007 chr6:30737225-30737234 chr6:30736997-30737006 chr6:30737222-30737231
43	BCL3	chr6:30749287-30750863	A549	lung:	n/a	chr6:30749933-30749942
44	BCL3	chr6:30736670-30737809	A549	lung:	n/a	chr6:30736998-30737007 chr6:30737225-30737234 chr6:30736997-30737006 chr6:30737222-30737231
45	BCLAF1	chr6:30735137-30735823	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:30749604-30750150	GM12878	blood:	n/a	chr6:30749933-30749942
47	BCLAF1	chr6:30735091-30735789	GM12878	blood:	n/a	n/a
48	BHLHE40	chr6:30731252-30731556	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:30753889-30753915	K562	blood:	n/a	n/a
50	BHLHE40	chr6:30735068-30735781	GM12878	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30740117-30740167	PANC-1	pancreas:	n/a
2	chr6:30740117-30740167	PANC-1	pancreas:	n/a
3	chr6:30749279-30749329	PANC-1	pancreas:	n/a
4	chr6:30737270-30737320	ECC-1	luminal epithelium:	n/a
5	chr6:30737455-30737505	SKMC	muscle:	n/a
6	chr6:30737270-30737320	AoSMC	blood vessel:	n/a
7	chr6:30737007-30737057	LNCaP	prostate:	n/a
8	chr6:30737231-30737281	SK-N-SH	brain:	n/a
9	chr6:30737068-30737118	Caco-2	colon:	n/a
10	chr6:30737455-30737505	NT2-D1	testis:	n/a
11	chr6:30737007-30737057	GM12891	blood:	n/a
12	chr6:30749279-30749329	BJ	skin:	n/a
13	chr6:30737231-30737281	AoSMC	blood vessel:	n/a
14	chr6:30737270-30737320	GM12892	blood:	n/a
15	chr6:30749279-30749329	NHBE	bronchial:	n/a
16	chr6:30737007-30737057	SAEC	small airway:	n/a
17	chr6:30749279-30749329	ECC-1	luminal epithelium:	n/a
18	chr6:30737231-30737281	HRCEpiC	kidney:	n/a
19	chr6:30749279-30749329	HCF	heart:	n/a
20	chr6:30737068-30737118	SK-N-SH	brain:	n/a
21	chr6:30737436-30737486	SKMC	muscle:	n/a
22	chr6:30737270-30737320	ProgFib	skin:	n/a
23	chr6:30737007-30737057	Hela-S3	cervix:	n/a
24	chr6:30737270-30737320	GM19239	blood:	n/a
25	chr6:30737231-30737281	RPTEC	kidney:	n/a
26	chr6:30737270-30737320	AG09309	skin:	n/a
27	chr6:30737231-30737281	MCF-7	breast:	n/a
28	chr6:30737068-30737118	PrEC	prostate:	n/a
29	chr6:30737436-30737486	HRPEpiC	eye:	n/a
30	chr6:30740117-30740167	HIPEpiC	eye:	n/a
31	chr6:30737270-30737320	LNCaP	prostate:	n/a
32	chr6:30737436-30737486	GM12891	blood:	n/a
33	chr6:30737068-30737118	SAEC	small airway:	n/a
34	chr6:30737270-30737320	RPTEC	kidney:	n/a
35	chr6:30737270-30737320	MCF10A-Er-Src	breast:	n/a
36	chr6:30737270-30737320	HL-60	blood:	n/a
37	chr6:30740117-30740167	IMR90	lung:	fetal
38	chr6:30749279-30749329	AG09309	skin:	n/a
39	chr6:30737270-30737320	NB4	blood:	n/a
40	chr6:30749279-30749329	GM19239	blood:	n/a
41	chr6:30737436-30737486	U87	brain:	n/a
42	chr6:30737270-30737320	HRE	kidney:	n/a
43	chr6:30737270-30737320	HAEpiC	amniotic membrane:	n/a
44	chr6:30740117-30740167	Hela-S3	cervix:	n/a
45	chr6:30737436-30737486	HCM	heart:	n/a
46	chr6:30740117-30740167	GM12878	blood:	n/a
47	chr6:30737068-30737118	LNCaP	prostate:	n/a
48	chr6:30737455-30737505	ProgFib	skin:	n/a
49	chr6:30737455-30737505	IMR90	lung:	fetal
50	chr6:30749279-30749329	AG09319	gingival:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:30746239..30748056-chr6:30850531..30852565,3	MCF-7	breast:
2	chr6:30709062..30712759-chr6:30740539..30742608,4	K562	blood:
3	chr6:30735343..30739242-chr6:30745410..30750382,5	MCF-7	breast:
4	chr6:30721626..30724111-chr6:30729705..30731621,2	K562	blood:
5	chr10:104401695..104404644-chr6:30737594..30739724,2	MCF-7	breast:
6	chr6:30738970..30741977-chr6:30793706..30796488,3	MCF-7	breast:
7	chr6:30711709..30712366-chr6:30736768..30737336,2	K562	blood:
8	chr6:30752526..30755713-chr6:30784163..30787914,3	MCF-7	breast:
9	chr6:30748393..30749996-chr6:30841265..30843895,2	K562	blood:
10	chr6:30649121..30651445-chr6:30738828..30742388,3	K562	blood:
11	chr6:30734711..30736301-chr6:30853270..30855138,2	MCF-7	breast:
12	chr6:30735516..30738178-chr6:30794315..30796554,3	MCF-7	breast:
13	chr14:69261158..69261792-chr6:30737040..30737774,2	Hela-S3	cervix:
14	chr6:30734934..30736907-chr6:30848739..30852223,3	MCF-7	breast:
15	chr6:30694210..30695985-chr6:30745346..30747310,2	K562	blood:
16	chr6:30685130..30687169-chr6:30748703..30751412,3	K562	blood:
17	chr6:30726903..30729816-chr6:30736090..30739671,3	K562	blood:
18	chr6:30639159..30640838-chr6:30736824..30738928,2	MCF-7	breast:
19	chr6:30735402..30739247-chr6:30785239..30791444,10	MCF-7	breast:
20	chr6:30745917..30748118-chr6:30776110..30778177,2	K562	blood:
21	chr6:30710566..30712092-chr6:30736043..30738574,2	K562	blood:
22	chr6:30725912..30728357-chr6:30744418..30747133,2	K562	blood:
23	chr6:30736036..30738964-chr6:30760194..30762277,2	K562	blood:
24	chr6:30718213..30720265-chr6:30735663..30737554,3	K562	blood:
25	chr6:30736584..30738500-chr6:30812126..30813733,2	MCF-7	breast:
26	chr6:30739130..30742242-chr6:30780166..30782431,3	K562	blood:
27	chr6:30735539..30738504-chr6:30880365..30881967,2	MCF-7	breast:
28	chr6:27100755..27102737-chr6:30749085..30751315,2	K562	blood:
29	chr6:30735949..30738859-chr6:30853029..30855349,2	MCF-7	breast:
30	chr6:30726903..30729816-chr6:30736090..30739671,3	K562	blood:
31	chr6:30583226..30586077-chr6:30737832..30742122,4	K562	blood:
32	chr6:30735125..30737471-chr6:30740402..30742755,2	MCF-7	breast:
33	chr6:30613838..30616795-chr6:30748344..30751338,2	K562	blood:
34	chr6:30583409..30587215-chr6:30748473..30750740,4	K562	blood:
35	chr6:30735347..30739906-chr6:30783605..30789456,10	MCF-7	breast:
36	chr6:30736125..30739794-chr6:30850488..30852740,4	MCF-7	breast:
37	chr6:30711510..30712566-chr6:30736765..30737864,4	Hela-S3	cervix:
38	chr6:30742016..30748001-chr6:30748066..30750476,5	MCF-7	breast:
39	chr6:30749778..30751326-chr6:30778307..30780023,3	MCF-7	breast:
40	chr6:30731319..30733794-chr6:30880499..30882436,2	K562	blood:
41	chr6:30729697..30732019-chr6:30764165..30766889,2	K562	blood:
42	chr6:30735613..30737637-chr6:30772309..30773867,2	MCF-7	breast:
43	chr6:30716396..30719291-chr6:30729856..30732825,2	K562	blood:
44	chr6:30713953..30715513-chr6:30740306..30742825,2	K562	blood:
45	chr6:30732229..30734221-chr6:30735941..30738002,2	K562	blood:
46	chr6:30688991..30691146-chr6:30731072..30732705,2	K562	blood:
47	chr6:30709664..30712008-chr6:30729353..30731357,3	K562	blood:
48	chr6:30739945..30741810-chr6:30780568..30783125,2	K562	blood:
49	chr6:30583545..30586231-chr6:30734562..30736210,2	K562	blood:
50	chr6:30749730..30752647-chr6:30754925..30756551,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TUBB-13	chr6:30749735-30749903	ENSG00000228022
2	lnc-TUBB-13	chr6:30734602-30734728	ENSG00000228022

No data

Variant related genes	Relation type
HCG20	TF binding region
HCG20	CpG island
ENSG00000204560	chromatin interactions
ENSG00000171206	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000204564	chromatin interactions
ENSG00000228022	chromatin interactions
ENSG00000137404	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000204599	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000180304	chromatin interactions
ENSG00000237775	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000257023	chromatin interactions
ENSG00000263608	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000196230	chromatin interactions
ENSG00000137411	chromatin interactions
ENSG00000266183	chromatin interactions
ENSG00000139163	chromatin interactions
ENSG00000272933	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000204568	chromatin interactions
ENSG00000222894	chromatin interactions
ENSG00000196787	chromatin interactions
ENSG00000204580	chromatin interactions
ENSG00000137337	chromatin interactions

Extended variants
information (count: 895 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11966040	chr6:30729487-30729488	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138090333	chr6:30729532-30729533	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs569614373	chr6:30729539-30729540	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs532031720	chr6:30729556-30729557	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs116095023	chr6:30729617-30729618	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs554808749	chr6:30729652-30729653	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs78008659	chr6:30729754-30729755	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs149541995	chr6:30729835-30729836	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs144105918	chr6:30729839-30729840	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs148719641	chr6:30729843-30729844	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs142298193	chr6:30729844-30729845	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs74455117	chr6:30729852-30729853	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs182500368	chr6:30729863-30729864	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs112417185	chr6:30729909-30729910	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs575967816	chr6:30729915-30729916	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs201259299	chr6:30729916-30729917	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs117471443	chr6:30730036-30730037	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs186819673	chr6:30730181-30730182	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs572164643	chr6:30730183-30730184	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs146299378	chr6:30730184-30730185	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs564026154	chr6:30730188-30730189	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs533041409	chr6:30730224-30730225	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs6926679	chr6:30730244-30730245	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs6926530	chr6:30730267-30730268	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs112323116	chr6:30730284-30730285	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs569007506	chr6:30730287-30730288	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs548919473	chr6:30730306-30730307	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs9262172	chr6:30730339-30730340	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs9262173	chr6:30730345-30730346	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs146613800	chr6:30730356-30730357	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs570897063	chr6:30730430-30730431	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs551171018	chr6:30730438-30730439	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs191383754	chr6:30730444-30730445	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs139847598	chr6:30730446-30730447	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs149854937	chr6:30730447-30730448	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs9262174	chr6:30730482-30730483	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs555253768	chr6:30730510-30730511	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs572261107	chr6:30730514-30730515	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs534559524	chr6:30730515-30730516	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs577723194	chr6:30730578-30730579	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs13213330	chr6:30730589-30730590	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs557629913	chr6:30730638-30730639	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs369920616	chr6:30730693-30730694	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs543519978	chr6:30730697-30730698	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs373096871	chr6:30730711-30730712	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs573693246	chr6:30730731-30730732	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs542604113	chr6:30730736-30730737	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs545284485	chr6:30730740-30730741	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs375890157	chr6:30730747-30730748	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs562247396	chr6:30730872-30730873	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	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
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30719800-30731600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr6:30720400-30731000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:30720600-30736600	Weak transcription	Gastric	stomach
4	chr6:30724000-30731400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:30725200-30729800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:30725400-30730000	Enhancers	Placenta Amnion	Placenta Amnion
7	chr6:30725600-30731000	Weak transcription	Primary T cells from cord blood	blood
8	chr6:30726200-30729800	Enhancers	HSMMtube	muscle
9	chr6:30726200-30730000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:30726400-30730200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:30726600-30729800	Enhancers	HMEC	breast
12	chr6:30726600-30729800	Enhancers	NHEK	skin
13	chr6:30726800-30731000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:30726800-30739000	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr6:30727200-30729800	Enhancers	Osteobl	bone
16	chr6:30727200-30730200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:30727200-30730400	Enhancers	A549	lung
18	chr6:30727200-30731000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr6:30727200-30731000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr6:30727200-30731200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr6:30727200-30731200	Weak transcription	K562	blood
22	chr6:30727400-30729600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr6:30727400-30731000	Enhancers	HepG2	liver
24	chr6:30727400-30731200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:30727600-30729800	Enhancers	Colon Smooth Muscle	Colon
26	chr6:30727600-30731200	Weak transcription	Fetal Stomach	stomach
27	chr6:30727800-30731000	Weak transcription	Fetal Intestine Small	intestine
28	chr6:30727800-30731400	Weak transcription	Fetal Muscle Leg	muscle
29	chr6:30728000-30731000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr6:30728000-30731200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:30728000-30731200	Weak transcription	Pancreas	Pancrea
32	chr6:30728000-30731200	Weak transcription	Right Atrium	heart
33	chr6:30728000-30731200	Weak transcription	HUVEC	blood vessel
34	chr6:30728000-30731400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:30728000-30731400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr6:30728000-30731600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:30728000-30731600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:30728000-30732800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr6:30728000-30737000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:30728200-30731000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr6:30728200-30731200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:30728200-30731200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:30728200-30731200	Weak transcription	Esophagus	oesophagus
44	chr6:30728200-30731200	Weak transcription	Placenta	Placenta
45	chr6:30728200-30731200	Weak transcription	Right Ventricle	heart
46	chr6:30728200-30731400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:30728200-30731400	Weak transcription	Left Ventricle	heart
48	chr6:30728200-30731400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr6:30728200-30731400	Weak transcription	HSMM	muscle
50	chr6:30728200-30731400	Weak transcription	NHLF	lung

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