Variant report

Variant	nsv886732
Chromosome Location	chr6:142290338-142536049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3067)
CpG islands
(count:2137)
Chromatin interactive
region (count:152)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3067 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:142330815-142331218	K562	blood:	n/a	n/a
2	ARID3A	chr6:142467784-142468437	K562	blood:	n/a	n/a
3	ARID3A	chr6:142467802-142468560	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:142433634-142433971	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:142509681-142509718	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:142310444-142310788	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:142528607-142528900	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:142492534-142492795	HepG2	liver:	n/a	n/a
9	ATF1	chr6:142351469-142351711	K562	blood:	n/a	n/a
10	ATF1	chr6:142332981-142333295	K562	blood:	n/a	n/a
11	ATF1	chr6:142468043-142468605	K562	blood:	n/a	n/a
12	ATF1	chr6:142330819-142331132	K562	blood:	n/a	n/a
13	ATF2	chr6:142468046-142468707	GM12878	blood:	n/a	n/a
14	ATF2	chr6:142467908-142468724	GM12878	blood:	n/a	n/a
15	ATF2	chr6:142334418-142334768	GM12878	blood:	n/a	n/a
16	ATF2	chr6:142334470-142334759	GM12878	blood:	n/a	n/a
17	ATF2	chr6:142468022-142468453	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr6:142409951-142410378	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr6:142310418-142310767	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:142467959-142468503	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr6:142334431-142334965	HCT-116	colon:	n/a	n/a
22	ATF3	chr6:142468119-142468361	K562	blood:	n/a	n/a
23	ATF3	chr6:142467960-142468496	A549	lung:	n/a	n/a
24	ATF3	chr6:142332913-142333217	K562	blood:	n/a	n/a
25	ATF3	chr6:142468001-142468494	K562	blood:	n/a	n/a
26	ATF3	chr6:142467971-142468588	A549	lung:	n/a	chr6:142468553-142468562
27	BACH1	chr6:142409357-142409582	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr6:142468027-142468472	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:142409948-142410277	H1-hESC	embryonic stem cell:	n/a	n/a
30	BATF	chr6:142468038-142468452	GM12878	blood:	n/a	n/a
31	BATF	chr6:142413816-142414046	GM12878	blood:	n/a	chr6:142413927-142413938
32	BATF	chr6:142376411-142376651	GM12878	blood:	n/a	n/a
33	BATF	chr6:142334510-142334762	GM12878	blood:	n/a	chr6:142334682-142334692
34	BATF	chr6:142413775-142414012	GM12878	blood:	n/a	chr6:142413927-142413938
35	BATF	chr6:142334507-142334749	GM12878	blood:	n/a	chr6:142334682-142334692
36	BCL11A	chr6:142334491-142334766	GM12878	blood:	n/a	chr6:142334680-142334689
37	BCL11A	chr6:142336110-142336403	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL3	chr6:142310499-142310930	GM12878	blood:	n/a	n/a
39	BCL3	chr6:142334415-142334778	GM12878	blood:	n/a	chr6:142334680-142334689
40	BCLAF1	chr6:142467982-142468621	GM12878	blood:	n/a	chr6:142468374-142468383
41	BCLAF1	chr6:142467900-142468691	GM12878	blood:	n/a	chr6:142468374-142468383
42	BCLAF1	chr6:142467983-142468766	K562	blood:	n/a	chr6:142468374-142468383
43	BCLAF1	chr6:142467910-142468518	K562	blood:	n/a	chr6:142468374-142468383
44	BHLHE40	chr6:142331333-142331472	K562	blood:	n/a	n/a
45	BHLHE40	chr6:142467972-142468783	K562	blood:	n/a	n/a
46	BHLHE40	chr6:142366125-142366500	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:142343404-142343413	K562	blood:	n/a	n/a
48	BHLHE40	chr6:142310528-142310763	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:142366123-142366493	GM12878	blood:	n/a	n/a
50	BHLHE40	chr6:142312127-142312290	GM12878	blood:	n/a	n/a

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142468354-142468404	GM06990	blood:	n/a
2	chr6:142410216-142410266	U87	brain:	n/a
3	chr6:142468354-142468404	GM06990	blood:	n/a
4	chr6:142410216-142410266	U87	brain:	n/a
5	chr6:142410221-142410271	LNCaP	prostate:	n/a
6	chr6:142468432-142468482	HMEC	breast:	n/a
7	chr6:142409831-142409881	NHBE	bronchial:	n/a
8	chr6:142410098-142410148	ovcar-3	ovarian:	n/a
9	chr6:142468318-142468368	SK-N-SH	brain:	n/a
10	chr6:142468318-142468368	PFSK-1	brain:	n/a
11	chr6:142468346-142468396	HEEpiC	esophagus:	n/a
12	chr6:142352423-142352473	Jurkat	blood:	n/a
13	chr6:142409507-142409557	K562	blood:	n/a
14	chr6:142409202-142409252	ProgFib	skin:	n/a
15	chr6:142468432-142468482	HCPEpiC	choroid plexus:	n/a
16	chr6:142468191-142468241	Hepatocyte	liver:	n/a
17	chr6:142409756-142409806	PANC-1	pancreas:	n/a
18	chr6:142409417-142409467	H1-hESC	embryonic stem cell:	embryo
19	chr6:142468356-142468406	HEEpiC	esophagus:	n/a
20	chr6:142413804-142413854	HL-60	blood:	n/a
21	chr6:142476640-142476690	HRPEpiC	eye:	n/a
22	chr6:142409507-142409557	HMEC	breast:	n/a
23	chr6:142352423-142352473	HMEC	breast:	n/a
24	chr6:142468318-142468368	IMR90	lung:	fetal
25	chr6:142352423-142352473	A549	lung:	n/a
26	chr6:142410235-142410285	T-47D	breast:	n/a
27	chr6:142352900-142352950	AG09319	gingival:	n/a
28	chr6:142409993-142410043	BJ	skin:	n/a
29	chr6:142468346-142468396	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:142409939-142409989	HNPCEpiC	eye:	n/a
31	chr6:142409939-142409989	MCF-7	breast:	n/a
32	chr6:142409202-142409252	NT2-D1	testis:	n/a
33	chr6:142409939-142409989	BJ	skin:	n/a
34	chr6:142409993-142410043	NB4	blood:	n/a
35	chr6:142467043-142467093	HRCEpiC	kidney:	n/a
36	chr6:142409630-142409680	BE2_C	brain:	n/a
37	chr6:142335484-142335534	PFSK-1	brain:	n/a
38	chr6:142409939-142409989	GM12892	blood:	n/a
39	chr6:142409756-142409806	H1-hESC	embryonic stem cell:	embryo
40	chr6:142409507-142409557	ovcar-3	ovarian:	n/a
41	chr6:142352423-142352473	Caco-2	colon:	n/a
42	chr6:142409756-142409806	A549	lung:	n/a
43	chr6:142468512-142468562	A549	lung:	n/a
44	chr6:142335484-142335534	HUVEC	blood vessel:	n/a
45	chr6:142468354-142468404	ovcar-3	ovarian:	n/a
46	chr6:142468197-142468247	GM12892	blood:	n/a
47	chr6:142335484-142335534	AG04449	skin:	fetal
48	chr6:142409756-142409806	HAEpiC	amniotic membrane:	n/a
49	chr6:142409507-142409557	A549	lung:	n/a
50	chr6:142409630-142409680	HEEpiC	esophagus:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:111980949..111982469-chr6:142364799..142366321,4	K562	blood:
2	chr11:69463942..69465442-chr6:142366315..142367823,2	K562	blood:
3	chr17:41398766..41402548-chr6:142364795..142367825,22	K562	blood:
4	chr17:41398742..41402600-chr6:142364799..142367825,21	K562	blood:
5	chr17:41380201..41383708-chr6:142364797..142367825,26	K562	blood:
6	chr12:77377724..77379224-chr6:142364821..142367801,2	K562	blood:
7	chr6:142470687..142472679-chr6:142481549..142483699,2	K562	blood:
8	chr6:142476386..142478985-chr6:142483280..142485789,2	MCF-7	breast:
9	chr17:41398699..41402637-chr6:142364804..142367821,8	MCF-7	breast:
10	chr6:142510733..142514047-chr6:142522766..142526301,3	K562	blood:
11	chr17:41399314..41402537-chr6:142366296..142367823,5	MCF-7	breast:
12	chr6:142366299..142366821-chrX:77931323..77931843,2	Hela-S3	cervix:
13	chr6:106716720..106717223-chr6:142365820..142366802,2	Hela-S3	cervix:
14	chr19:49942462..49943984-chr6:142364795..142366315,3	K562	blood:
15	chr17:41391026..41393127-chr6:142366322..142367825,2	K562	blood:
16	chr13:52409628..52411128-chr6:142364817..142366324,2	MCF-7	breast:
17	chr6:142342024..142345729-chr6:142348880..142352239,3	K562	blood:
18	chr17:41391510..41393303-chr6:142364805..142367822,3	K562	blood:
19	chr6:142310160..142310940-chr6:142392407..142393314,2	MCF-7	breast:
20	chr6:142309853..142311057-chr6:142366249..142367364,12	MCF-7	breast:
21	chr6:142310115..142310645-chr6:142364498..142365481,2	MCF-7	breast:
22	chr6:142311068..142312761-chr6:142315282..142317322,2	K562	blood:
23	chr6:142472276..142475078-chr6:142622089..142623666,2	MCF-7	breast:
24	chr11:62607631..62609197-chr6:142364799..142366321,4	MCF-7	breast:
25	chr6:142477318..142478226-chr6:142708979..142709556,2	MCF-7	breast:
26	chr6:142475480..142479893-chr6:142481592..142484800,4	K562	blood:
27	chr11:62607617..62610628-chr6:142364795..142367820,5	K562	blood:
28	chr2:169365139..169366658-chr6:142364815..142367814,2	K562	blood:
29	chr6:142388215..142391078-chr6:142393829..142396159,2	K562	blood:
30	chr6:142481873..142484319-chr6:142484922..142487226,2	MCF-7	breast:
31	chr6:142366316..142367825-chrX:77930343..77931843,2	K562	blood:
32	chr20:18807037..18808557-chr6:142364804..142366320,2	MCF-7	breast:
33	chr6:142365543..142367464-chr6:142370102..142372383,2	K562	blood:
34	chr6:141998099..141999007-chr6:142433461..142433965,2	MCF-7	breast:
35	chr6:141996747..141997654-chr6:142433323..142434142,3	MCF-7	breast:
36	chr6:142310081..142310988-chr6:142433318..142434235,4	K562	blood:
37	chr6:142310160..142310940-chr6:142392407..142393314,2	MCF-7	breast:
38	chr6:142301363..142303656-chr6:142306622..142308997,2	MCF-7	breast:
39	chr6:4691449..4692204-chr6:142470501..142471255,2	MCF-7	breast:
40	chr2:137557381..137558381-chr6:142365795..142366315,2	Hela-S3	cervix:
41	chr17:41380544..41383110-chr6:142366321..142367825,2	MCF-7	breast:
42	chr6:141998374..141999368-chr6:142433353..142434249,2	MCF-7	breast:
43	chr3:73159944..73162090-chr6:142364797..142366302,3	MCF-7	breast:
44	chr6:142480480..142482070-chr6:142484857..142487134,2	MCF-7	breast:
45	chr6:142510733..142514047-chr6:142522766..142526301,3	K562	blood:
46	chr6:142470687..142472679-chr6:142481549..142483699,2	K562	blood:
47	chr6:142366297..142366805-chr8:21899435..21899935,2	Hela-S3	cervix:
48	chr6:142470468..142472219-chr6:144162798..144164527,2	K562	blood:
49	chr6:142345393..142347515-chr6:142353520..142355700,2	K562	blood:
50	chr6:142528358..142528953-chr6:142709482..142710029,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJE1-4	chr6:142496680-142496862	NONHSAT115305
2	lnc-GJE1-6	chr6:142383854-142384190	NONHSAT115302
3	lnc-GJE1-4	chr6:142495920-142496027	NONHSAT115305
4	lnc-GJE1-4	chr6:142497360-142497981	NONHSAT115305

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VTA1	hsa-miR-455-5p	chr6:142510580-142510603

Variant related genes	Relation type
ENSG00000270983	TF binding region
GJE1	TF binding region
VTA1	TF binding region
ENSG00000236822	TF binding region
NMBR	TF binding region
ENSG00000270983	CpG island
GJE1	CpG island
VTA1	CpG island
ENSG00000236822	CpG island
NMBR	CpG island
ENSG00000257199	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000173852	chromatin interactions
ENSG00000104907	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000009844	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000104888	chromatin interactions
ENSG00000112414	chromatin interactions
ENSG00000158815	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000135521	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000270983	chromatin interactions

Extended variants
information (count: 6215 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:6215 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554436943	chr6:142290338-142290339	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376545900	chr6:142290342-142290343	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71021644	chr6:142290343-142290344	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs60147541	chr6:142290344-142290345	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201734934	chr6:142290350-142290351	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539007053	chr6:142290389-142290390	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562456684	chr6:142290390-142290391	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533687528	chr6:142290410-142290411	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs372136172	chr6:142290436-142290437	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs552066605	chr6:142290439-142290440	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs560749832	chr6:142290449-142290450	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs377532672	chr6:142290535-142290536	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs9496207	chr6:142290540-142290541	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs571957603	chr6:142290554-142290555	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs573318629	chr6:142290568-142290569	Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs142948590	chr6:142290634-142290635	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111338110	chr6:142290635-142290636	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183572065	chr6:142290637-142290638	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549913399	chr6:142290658-142290659	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557617363	chr6:142290659-142290660	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571590338	chr6:142290661-142290662	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114272215	chr6:142290664-142290665	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7755011	chr6:142290671-142290672	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188020744	chr6:142290685-142290686	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559166963	chr6:142290686-142290687	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555497332	chr6:142290714-142290715	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113569503	chr6:142290719-142290720	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544767117	chr6:142290724-142290725	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544265699	chr6:142290731-142290732	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562358885	chr6:142290736-142290737	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577745881	chr6:142290761-142290762	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139300885	chr6:142290765-142290766	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560810787	chr6:142290767-142290768	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527984574	chr6:142290784-142290785	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549323066	chr6:142290802-142290803	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561488652	chr6:142290811-142290812	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs531736364	chr6:142290826-142290827	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550215642	chr6:142290829-142290830	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149600607	chr6:142290836-142290837	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369446774	chr6:142290846-142290847	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532399226	chr6:142290854-142290855	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547385016	chr6:142290910-142290911	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566439289	chr6:142290920-142290921	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556187861	chr6:142290935-142290936	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138109469	chr6:142290937-142290938	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144015653	chr6:142290942-142290943	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148232186	chr6:142290967-142290968	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs139469628	chr6:142290970-142290971	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139937144	chr6:142290971-142290972	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537626357	chr6:142290983-142290984	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Autism	22495311	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
Gastric cancer	17908304	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
Colorectal cancer	16272173	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Burkitt''s lymphoma	19759907	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2964 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142284400-142292000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:142289600-142290600	Flanking Active TSS	Liver	Liver
3	chr6:142289800-142290400	Enhancers	Fetal Heart	heart
4	chr6:142290200-142290400	Enhancers	Hela-S3	cervix
5	chr6:142290400-142291200	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr6:142290400-142291200	Active TSS	Hela-S3	cervix
7	chr6:142290600-142290800	Enhancers	Liver	Liver
8	chr6:142290800-142291000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:142290800-142291200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr6:142291600-142291800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:142301800-142302000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr6:142302400-142302600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr6:142302600-142302800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:142302600-142302800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr6:142302600-142304800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr6:142302800-142310600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr6:142304600-142304800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:142304800-142305000	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:142304800-142306200	Enhancers	Placenta Amnion	Placenta Amnion
20	chr6:142304800-142316000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr6:142305000-142305800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr6:142305000-142306000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr6:142305600-142305800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr6:142305600-142306000	Enhancers	Fetal Heart	heart
25	chr6:142305800-142306000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr6:142305800-142306000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:142305800-142306200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr6:142306000-142306200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:142306000-142307600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr6:142306000-142310200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr6:142306200-142310200	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr6:142306200-142310400	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr6:142307600-142308000	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr6:142307800-142308000	Enhancers	Pancreas	Pancrea
35	chr6:142307800-142309000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:142307800-142309200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr6:142307800-142309800	Enhancers	Liver	Liver
38	chr6:142308000-142310200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr6:142309000-142309200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:142309000-142310200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr6:142309200-142310000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr6:142309200-142310200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr6:142309800-142310600	Flanking Active TSS	Liver	Liver
44	chr6:142310000-142310200	Enhancers	NHDF-Ad	bronchial
45	chr6:142310000-142312200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr6:142310000-142312200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:142310200-142310400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:142310200-142310600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr6:142310200-142310800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr6:142310200-142310800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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