Variant report

Variant	esv3528473
Chromosome Location	chr14:37631543-37771255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2207)
CpG islands
(count:1527)
Chromatin interactive
region (count:143)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:37664464-37664897	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:37747860-37748994	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:37640896-37641730	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:37636859-37637271	K562	blood:	n/a	n/a
5	ARID3A	chr14:37642484-37642976	K562	blood:	n/a	n/a
6	ARID3A	chr14:37668114-37668178	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:37699763-37700208	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:37640439-37641338	K562	blood:	n/a	n/a
9	ARID3A	chr14:37702174-37702457	K562	blood:	n/a	n/a
10	ARID3A	chr14:37667012-37667537	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:37715436-37716157	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:37637980-37638323	K562	blood:	n/a	n/a
13	ARID3A	chr14:37643767-37644084	K562	blood:	n/a	n/a
14	ARID3A	chr14:37699852-37700129	K562	blood:	n/a	n/a
15	ARID3A	chr14:37641543-37641674	K562	blood:	n/a	n/a
16	ARID3A	chr14:37702064-37702476	HepG2	liver:	n/a	n/a
17	ARID3A	chr14:37665962-37666204	K562	blood:	n/a	n/a
18	ARID3A	chr14:37638798-37638998	K562	blood:	n/a	chr14:37638878-37638894 chr14:37638877-37638893
19	ARID3A	chr14:37720992-37722152	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:37739891-37740124	HepG2	liver:	n/a	n/a
21	ARID3A	chr14:37707129-37707415	HepG2	liver:	n/a	n/a
22	ARID3A	chr14:37636253-37636339	K562	blood:	n/a	n/a
23	ARID3A	chr14:37666578-37667618	K562	blood:	n/a	n/a
24	ATF1	chr14:37637957-37638275	K562	blood:	n/a	n/a
25	ATF1	chr14:37636855-37637252	K562	blood:	n/a	n/a
26	ATF2	chr14:37636749-37637333	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr14:37641089-37641818	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr14:37636807-37637410	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr14:37641468-37642010	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr14:37650651-37650943	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr14:37666986-37667277	K562	blood:	n/a	n/a
32	ATF3	chr14:37641048-37641567	A549	lung:	n/a	n/a
33	ATF3	chr14:37639465-37639767	K562	blood:	n/a	n/a
34	BACH1	chr14:37641174-37642006	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr14:37667015-37667867	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr14:37636808-37637367	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr14:37636967-37637160	K562	blood:	n/a	n/a
38	BACH1	chr14:37666966-37667533	K562	blood:	n/a	n/a
39	BCL3	chr14:37641013-37641625	A549	lung:	n/a	n/a
40	BCL3	chr14:37640978-37641543	A549	lung:	n/a	n/a
41	BCLAF1	chr14:37640954-37641540	K562	blood:	n/a	n/a
42	BHLHE40	chr14:37702192-37702420	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:37641028-37642076	K562	blood:	n/a	n/a
44	BHLHE40	chr14:37715661-37715909	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:37666734-37667614	K562	blood:	n/a	n/a
46	BHLHE40	chr14:37702149-37702324	K562	blood:	n/a	n/a
47	BHLHE40	chr14:37637932-37638567	K562	blood:	n/a	n/a
48	BRCA1	chr14:37667409-37667484	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr14:37641134-37641473	HepG2	liver:	n/a	n/a
50	BRCA1	chr14:37666826-37667336	HepG2	liver:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:37667689-37667739	SK-N-SH_RA	brain:	n/a
2	chr14:37644675-37644725	BJ	skin:	n/a
3	chr14:37667689-37667739	SK-N-SH_RA	brain:	n/a
4	chr14:37644675-37644725	BJ	skin:	n/a
5	chr14:37641436-37641486	MCF-7	breast:	n/a
6	chr14:37641134-37641184	AoSMC	blood vessel:	n/a
7	chr14:37641660-37641710	HIPEpiC	eye:	n/a
8	chr14:37666893-37666943	AG09319	gingival:	n/a
9	chr14:37664088-37664138	SK-N-MC	brain:	n/a
10	chr14:37667230-37667280	HCT-116	colon:	n/a
11	chr14:37640247-37640297	IMR90	lung:	fetal
12	chr14:37666920-37666970	AG10803	skin:	n/a
13	chr14:37667261-37667311	HUVEC	blood vessel:	n/a
14	chr14:37644675-37644725	GM12892	blood:	n/a
15	chr14:37640247-37640297	GM19239	blood:	n/a
16	chr14:37641660-37641710	AG10803	skin:	n/a
17	chr14:37664088-37664138	HEEpiC	esophagus:	n/a
18	chr14:37641191-37641241	ECC-1	luminal epithelium:	n/a
19	chr14:37641462-37641512	A549	lung:	n/a
20	chr14:37641191-37641241	AG10803	skin:	n/a
21	chr14:37666893-37666943	AG10803	skin:	n/a
22	chr14:37640455-37640505	SK-N-MC	brain:	n/a
23	chr14:37666810-37666860	HCPEpiC	choroid plexus:	n/a
24	chr14:37664088-37664138	SKMC	muscle:	n/a
25	chr14:37666994-37667044	AG10803	skin:	n/a
26	chr14:37664088-37664138	H1-hESC	embryonic stem cell:	embryo
27	chr14:37641134-37641184	Caco-2	colon:	n/a
28	chr14:37667261-37667311	SK-N-MC	brain:	n/a
29	chr14:37666920-37666970	BE2_C	brain:	n/a
30	chr14:37667833-37667883	HPAEpiC	pulmonary alveolar:	n/a
31	chr14:37666994-37667044	K562	blood:	n/a
32	chr14:37666931-37666981	Hepatocyte	liver:	n/a
33	chr14:37666931-37666981	Hela-S3	cervix:	n/a
34	chr14:37641191-37641241	HMEC	breast:	n/a
35	chr14:37666994-37667044	A549	lung:	n/a
36	chr14:37667261-37667311	NHDF-neo	bronchial:	n/a
37	chr14:37644675-37644725	PrEC	prostate:	n/a
38	chr14:37670820-37670870	Jurkat	blood:	n/a
39	chr14:37667230-37667280	T-47D	breast:	n/a
40	chr14:37666931-37666981	MCF10A-Er-Src	breast:	n/a
41	chr14:37640455-37640505	SKMC	muscle:	n/a
42	chr14:37641261-37641311	MCF-7	breast:	n/a
43	chr14:37667261-37667311	AG09319	gingival:	n/a
44	chr14:37666931-37666981	CMK	blood:	n/a
45	chr14:37667261-37667311	Hepatocyte	liver:	n/a
46	chr14:37641964-37642014	Jurkat	blood:	n/a
47	chr14:37641726-37641776	GM06990	blood:	n/a
48	chr14:37667689-37667739	Jurkat	blood:	n/a
49	chr14:37641660-37641710	H1-hESC	embryonic stem cell:	embryo
50	chr14:37664088-37664138	U87	brain:	n/a

(count:143 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:37743207..37745238-chr14:37747689..37750127,2	MCF-7	breast:
2	chr14:37703862..37705867-chr14:38056619..38058843,2	MCF-7	breast:
3	chr14:37696817..37699280-chr14:37707291..37710248,2	MCF-7	breast:
4	chr14:37723534..37725938-chr14:37730959..37732560,2	K562	blood:
5	chr14:37697471..37699396-chr14:38051501..38053443,2	MCF-7	breast:
6	chr14:37635891..37637422-chr14:37666864..37668416,2	MCF-7	breast:
7	chr14:37649527..37651591-chr14:37665474..37668533,3	MCF-7	breast:
8	chr14:37700806..37703619-chr14:37711035..37714311,4	MCF-7	breast:
9	chr14:37051690..37053277-chr14:37640298..37642030,2	K562	blood:
10	chr14:37641298..37642813-chr14:37662827..37664578,2	MCF-7	breast:
11	chr14:37697269..37708885-chr14:38056043..38068163,30	MCF-7	breast:
12	chr14:37639061..37645694-chr14:37661777..37669317,18	MCF-7	breast:
13	chr14:37639697..37645467-chr14:37664720..37672395,14	K562	blood:
14	chr14:37641268..37642823-chr14:37697545..37700025,2	MCF-7	breast:
15	chr14:37662314..37664941-chr14:37664960..37666969,2	K562	blood:
16	chr14:37641825..37643910-chr14:37649630..37653751,3	K562	blood:
17	chr14:37680569..37683226-chr14:37683414..37685864,2	MCF-7	breast:
18	chr14:37704717..37707352-chr14:38053028..38056563,4	MCF-7	breast:
19	chr14:37640543..37642943-chr20:48598351..48600093,2	MCF-7	breast:
20	chr14:37688098..37689873-chr14:37692378..37694206,2	MCF-7	breast:
21	chr14:37639061..37645694-chr14:37661777..37669317,18	MCF-7	breast:
22	chr14:37640829..37643687-chr14:37650994..37653256,2	K562	blood:
23	chr14:37680569..37683226-chr14:37683414..37685864,2	MCF-7	breast:
24	chr14:37665713..37668591-chr14:37669501..37671550,2	K562	blood:
25	chr14:37720431..37722161-chr14:37725187..37727828,2	MCF-7	breast:
26	chr14:37719816..37722174-chr14:38034571..38037096,4	MCF-7	breast:
27	chr14:37724973..37727829-chr14:37731230..37733021,2	MCF-7	breast:
28	chr14:37638286..37642814-chr14:37645632..37648854,6	K562	blood:
29	chr14:37734748..37736405-chr14:37736490..37738328,2	MCF-7	breast:
30	chr14:37713685..37715772-chr14:37718261..37720705,2	K562	blood:
31	chr14:37723949..37726058-chr14:37737860..37739770,2	MCF-7	breast:
32	chr14:37724664..37726988-chr14:38331777..38333562,2	MCF-7	breast:
33	chr14:37667188..37668774-chr14:37681989..37684290,2	K562	blood:
34	chr14:37439762..37441841-chr14:37637700..37639770,2	K562	blood:
35	chr14:37639697..37645467-chr14:37664720..37672395,14	K562	blood:
36	chr14:37723949..37726058-chr14:37737860..37739770,2	MCF-7	breast:
37	chr14:37666447..37670165-chr14:37687994..37691286,5	MCF-7	breast:
38	chr14:37713685..37715695-chr14:37718418..37720705,2	K562	blood:
39	chr14:37713685..37715772-chr14:37718261..37720705,2	K562	blood:
40	chr14:37638513..37640081-chr14:37646893..37648669,2	MCF-7	breast:
41	chr14:37619150..37623313-chr14:37636849..37639143,3	K562	blood:
42	chr14:37743207..37745238-chr14:37747689..37750127,2	MCF-7	breast:
43	chr14:37667088..37669471-chr14:37678201..37679725,2	K562	blood:
44	chr14:37672188..37673767-chr14:37677538..37679060,2	K562	blood:
45	chr14:37720431..37722161-chr14:37725187..37727828,2	MCF-7	breast:
46	chr14:37666297..37668856-chr14:38035873..38037389,2	MCF-7	breast:
47	chr14:37720865..37721694-chr14:38063366..38064030,2	MCF-7	breast:
48	chr14:37619842..37620362-chr14:37699681..37700515,2	K562	blood:
49	chr14:37641949..37644227-chr14:37646563..37648217,2	MCF-7	breast:
50	chr14:37699430..37701952-chr14:37706278..37708031,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MIPOL1-5	chr14:37641231-37642998	NR_033240
2	lnc-RP11-537P22.1.1-1	chr14:37736143-37736374	NONHSAT036456
3	lnc-RP11-537P22.1.1-1	chr14:37716308-37716445	NONHSAT036456
4	lnc-RP11-537P22.1.1-1	chr14:37727929-37730334	NONHSAT036457
5	lnc-RP11-537P22.1.1-1	chr14:37709629-37709774	NONHSAT036456
6	lnc-RP11-537P22.1.1-1	chr14:37717034-37717112	NONHSAT036456
7	lnc-RP11-537P22.1.1-1	chr14:37737668-37742505	l_969_chr14:37729807-37741737_76bGuttman_hES
8	lnc-RP11-537P22.1.1-1	chr14:37732158-37732474	l_969_chr14:37729807-37741737_76bGuttman_hES
9	lnc-RP11-537P22.1.1-1	chr14:37729808-37730221	l_969_chr14:37729807-37741737_76bGuttman_hES
10	lnc-RP11-537P22.1.1-1	chr14:37734270-37737659	l_969_chr14:37729807-37741737_76bGuttman_hES

No data

Variant related genes	Relation type
MIPOL1	TF binding region
SLC25A21-AS1	TF binding region
SLC25A21	TF binding region
RNU6-273P	TF binding region
MIPOL1	CpG island
SLC25A21-AS1	CpG island
SLC25A21	CpG island
RNU6-273P	CpG island
ENSG00000124216	chromatin interactions
ENSG00000259087	chromatin interactions
ENSG00000258414	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000258708	chromatin interactions
ENSG00000183032	chromatin interactions
ENSG00000151338	chromatin interactions
ENSG00000107338	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000255872	chromatin interactions
ENSG00000136327	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000198807	chromatin interactions

Extended variants
information (count: 5058 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:5058 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201468872	chr14:37631546-37631547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs187261722	chr14:37631585-37631586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375810666	chr14:37631587-37631588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7152257	chr14:37631599-37631600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192947040	chr14:37631624-37631625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141572549	chr14:37631789-37631790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150890533	chr14:37631806-37631807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7153106	chr14:37631819-37631820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369267248	chr14:37631885-37631886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558507555	chr14:37631901-37631902	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs571242745	chr14:37631931-37631932	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533851052	chr14:37631996-37631997	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372701661	chr14:37632095-37632096	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs8020903	chr14:37632288-37632289	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs149274064	chr14:37632340-37632341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs542417021	chr14:37632381-37632382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs8019950	chr14:37632402-37632403	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs556263880	chr14:37632458-37632459	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs372755550	chr14:37632490-37632491	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376253733	chr14:37632491-37632492	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs375063885	chr14:37632499-37632500	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559251768	chr14:37632500-37632501	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575282036	chr14:37632503-37632504	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs554365958	chr14:37632507-37632508	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs34749912	chr14:37632522-37632523	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs199516621	chr14:37632525-37632526	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576053202	chr14:37632533-37632534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs185501560	chr14:37632561-37632562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs190347414	chr14:37632564-37632565	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs527244759	chr14:37632578-37632579	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541751791	chr14:37632665-37632666	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561527919	chr14:37632694-37632695	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs530361729	chr14:37632695-37632696	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs572270403	chr14:37632831-37632832	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570160478	chr14:37632855-37632856	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551070144	chr14:37632895-37632896	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560184117	chr14:37632920-37632921	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs193299616	chr14:37632931-37632932	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552220621	chr14:37632950-37632951	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs10130026	chr14:37632967-37632968	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534652876	chr14:37633003-37633004	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs183698530	chr14:37633056-37633057	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs567438102	chr14:37633079-37633080	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547150236	chr14:37633129-37633130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75894468	chr14:37633154-37633155	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs188415533	chr14:37633155-37633156	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs10130470	chr14:37633184-37633185	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs536172534	chr14:37633185-37633186	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139534792	chr14:37633298-37633299	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs558655045	chr14:37633321-37633322	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1237 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37630000-37638000	Weak transcription	Pancreas	Pancrea
2	chr14:37631200-37635000	Weak transcription	K562	blood
3	chr14:37631600-37636200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr14:37634800-37635600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:37635000-37635200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr14:37635000-37636800	Enhancers	K562	blood
7	chr14:37635200-37635400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr14:37635200-37636200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr14:37635200-37636800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr14:37635400-37636400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr14:37635600-37636000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr14:37636000-37636800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr14:37636000-37638600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr14:37636200-37637200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr14:37636200-37637200	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr14:37636400-37638600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr14:37636400-37638600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr14:37636400-37638800	Enhancers	H1 Cell Line	embryonic stem cell
19	chr14:37636400-37638800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr14:37636600-37637200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr14:37636800-37637000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
22	chr14:37636800-37637000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr14:37636800-37637000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr14:37636800-37639000	Flanking Active TSS	K562	blood
25	chr14:37637000-37637200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr14:37637000-37637200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr14:37637200-37637400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr14:37637200-37637600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr14:37637200-37637600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr14:37637200-37637600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr14:37637200-37637600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr14:37637200-37638000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr14:37637200-37638200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr14:37637400-37638200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr14:37637600-37638400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr14:37637600-37638600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr14:37637600-37638600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr14:37637600-37639000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr14:37637800-37638000	Enhancers	Fetal Heart	heart
40	chr14:37637800-37638400	Enhancers	Duodenum Mucosa	Duodenum
41	chr14:37638000-37638600	Enhancers	Pancreas	Pancrea
42	chr14:37638000-37638800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr14:37638000-37639000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr14:37638200-37638400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr14:37638200-37638400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr14:37638200-37638600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr14:37638400-37638600	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr14:37638400-37640800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr14:37638400-37641000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr14:37638600-37638800	Enhancers	Small Intestine	intestine

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