Variant report

Variant	nsv583153
Chromosome Location	chr2:133167263-133361282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1703)
CpG islands
(count:2020)
Chromatin interactive
region (count:75)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1703 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:133304875-133304890	K562	blood:	n/a	n/a
2	ARID3A	chr2:133174024-133174324	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:133182024-133182468	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:133304775-133304963	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:133206471-133206700	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:133197370-133197703	HepG2	liver:	n/a	n/a
7	ATF3	chr2:133173868-133174360	A549	lung:	n/a	n/a
8	ATF3	chr2:133196210-133196622	A549	lung:	n/a	n/a
9	BACH1	chr2:133173941-133174219	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr2:133173475-133174583	A549	lung:	n/a	chr2:133174091-133174104 chr2:133174016-133174025 chr2:133174107-133174120 chr2:133173569-133173578
11	BCL3	chr2:133196228-133196753	A549	lung:	n/a	chr2:133196462-133196471
12	BCL3	chr2:133196055-133196767	A549	lung:	n/a	chr2:133196462-133196471
13	BCL3	chr2:133173786-133174427	A549	lung:	n/a	chr2:133174091-133174104 chr2:133174016-133174025 chr2:133174107-133174120
14	BHLHE40	chr2:133197341-133197721	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:133174899-133175021	K562	blood:	n/a	n/a
16	BHLHE40	chr2:133174028-133174155	K562	blood:	n/a	n/a
17	BHLHE40	chr2:133175471-133175541	K562	blood:	n/a	n/a
18	BHLHE40	chr2:133187043-133187166	K562	blood:	n/a	n/a
19	BHLHE40	chr2:133173885-133174262	HepG2	liver:	n/a	chr2:133173990-133174006 chr2:133173975-133173991
20	BRCA1	chr2:133174120-133174267	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr2:133196024-133196837	HCT-116	colon:	n/a	n/a
22	CEBPB	chr2:133172875-133173231	HepG2	liver:	n/a	chr2:133173034-133173045
23	CEBPB	chr2:133195547-133195632	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:133204426-133204623	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:133173813-133174515	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr2:133200727-133201051	A549	lung:	n/a	chr2:133200853-133200864
27	CEBPB	chr2:133280625-133280665	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:133189784-133190098	HepG2	liver:	n/a	chr2:133189927-133189938
29	CEBPB	chr2:133347693-133347799	IMR90	lung:	n/a	n/a
30	CEBPB	chr2:133231795-133231925	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:133196084-133196752	A549	lung:	n/a	n/a
32	CEBPB	chr2:133197407-133197648	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:133172679-133173262	IMR90	lung:	n/a	chr2:133173034-133173045
34	CEBPB	chr2:133189867-133190069	A549	lung:	n/a	chr2:133189927-133189938
35	CEBPB	chr2:133325972-133325984	A549	lung:	n/a	n/a
36	CEBPB	chr2:133200725-133201046	HepG2	liver:	n/a	chr2:133200853-133200864
37	CEBPB	chr2:133181293-133181385	A549	lung:	n/a	n/a
38	CEBPB	chr2:133173960-133174204	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:133325882-133326055	HepG2	liver:	n/a	chr2:133325967-133325978
40	CEBPB	chr2:133333363-133333495	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:133204360-133204566	A549	lung:	n/a	n/a
42	CEBPB	chr2:133206407-133206723	MCF-7	breast:	n/a	n/a
43	CEBPB	chr2:133196295-133196542	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:133189883-133190087	IMR90	lung:	n/a	chr2:133189927-133189938
45	CEBPB	chr2:133333292-133333484	A549	lung:	n/a	n/a
46	CEBPB	chr2:133172939-133173163	H1-hESC	embryonic stem cell:	n/a	chr2:133173034-133173045
47	CEBPB	chr2:133319880-133320042	IMR90	lung:	n/a	n/a
48	CEBPB	chr2:133200681-133201013	A549	lung:	n/a	chr2:133200853-133200864
49	CEBPB	chr2:133181936-133182384	MCF-7	breast:	n/a	n/a
50	CEBPB	chr2:133182022-133182810	HepG2	liver:	n/a	chr2:133182631-133182642

(count:2020 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133175382-133175432	HCT-116	colon:	n/a
2	chr2:133342286-133342336	T-47D	breast:	n/a
3	chr2:133343657-133343707	SK-N-MC	brain:	n/a
4	chr2:133175192-133175242	IMR90	lung:	fetal
5	chr2:133174035-133174085	GM12892	blood:	n/a
6	chr2:133174035-133174085	MCF10A-Er-Src	breast:	n/a
7	chr2:133189699-133189749	HEK293	kidney:	embryo
8	chr2:133175382-133175432	HCT-116	colon:	n/a
9	chr2:133342286-133342336	T-47D	breast:	n/a
10	chr2:133343657-133343707	SK-N-MC	brain:	n/a
11	chr2:133175192-133175242	IMR90	lung:	fetal
12	chr2:133174035-133174085	GM12892	blood:	n/a
13	chr2:133174035-133174085	MCF10A-Er-Src	breast:	n/a
14	chr2:133189699-133189749	HEK293	kidney:	embryo
15	chr2:133175382-133175432	SK-N-SH_RA	brain:	n/a
16	chr2:133189699-133189749	SAEC	small airway:	n/a
17	chr2:133342286-133342336	HPAEpiC	pulmonary alveolar:	n/a
18	chr2:133189699-133189749	RPTEC	kidney:	n/a
19	chr2:133173718-133173768	AG04449	skin:	fetal
20	chr2:133342286-133342336	GM12891	blood:	n/a
21	chr2:133171941-133171991	SK-N-SH	brain:	n/a
22	chr2:133173643-133173693	PFSK-1	brain:	n/a
23	chr2:133175382-133175432	HRE	kidney:	n/a
24	chr2:133343618-133343668	SK-N-SH_RA	brain:	n/a
25	chr2:133175382-133175432	BE2_C	brain:	n/a
26	chr2:133174094-133174144	Caco-2	colon:	n/a
27	chr2:133174035-133174085	RPTEC	kidney:	n/a
28	chr2:133343618-133343668	AG10803	skin:	n/a
29	chr2:133342286-133342336	K562	blood:	n/a
30	chr2:133343657-133343707	HRCEpiC	kidney:	n/a
31	chr2:133174035-133174085	ProgFib	skin:	n/a
32	chr2:133343373-133343423	HPAEpiC	pulmonary alveolar:	n/a
33	chr2:133175192-133175242	PFSK-1	brain:	n/a
34	chr2:133174117-133174167	HMEC	breast:	n/a
35	chr2:133175311-133175361	CMK	blood:	n/a
36	chr2:133342286-133342336	HCPEpiC	choroid plexus:	n/a
37	chr2:133343628-133343678	GM06990	blood:	n/a
38	chr2:133174094-133174144	HRPEpiC	eye:	n/a
39	chr2:133343657-133343707	HCF	heart:	n/a
40	chr2:133176249-133176299	SAEC	small airway:	n/a
41	chr2:133197577-133197627	AoSMC	blood vessel:	n/a
42	chr2:133171941-133171991	RPTEC	kidney:	n/a
43	chr2:133178190-133178240	Hela-S3	cervix:	n/a
44	chr2:133174635-133174685	HRPEpiC	eye:	n/a
45	chr2:133342286-133342336	AG10803	skin:	n/a
46	chr2:133175311-133175361	Hepatocyte	liver:	n/a
47	chr2:133171381-133171431	NHBE	bronchial:	n/a
48	chr2:133343308-133343358	HCT-116	colon:	n/a
49	chr2:133173533-133173583	HEK293	kidney:	embryo
50	chr2:133343115-133343165	HRPEpiC	eye:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:133304031..133305145-chr2:133928594..133929580,6	MCF-7	breast:
2	chr2:133274709..133277168-chr2:133277775..133280190,2	K562	blood:
3	chr2:133174216..133177088-chr2:133183800..133185718,2	MCF-7	breast:
4	chr2:133274387..133277041-chr2:133279166..133281960,2	MCF-7	breast:
5	chr2:133183645..133185687-chr2:133186251..133189764,3	MCF-7	breast:
6	chr2:133339874..133340573-chr2:133634427..133634936,2	MCF-7	breast:
7	chr2:133230048..133232279-chr2:133233399..133234934,2	MCF-7	breast:
8	chr2:133218079..133220375-chr2:133221168..133223212,2	MCF-7	breast:
9	chr2:133330055..133331591-chr2:133427502..133429942,2	MCF-7	breast:
10	chr2:133304368..133305326-chr2:134601553..134602523,5	K562	blood:
11	chr2:133164142..133169602-chr2:133170573..133175419,7	MCF-7	breast:
12	chr2:133183645..133185687-chr2:133186251..133189764,3	MCF-7	breast:
13	chr2:133304762..133308062-chr2:133425978..133429369,3	MCF-7	breast:
14	chr2:133304876..133306446-chr2:133426520..133428307,2	MCF-7	breast:
15	chr2:133183721..133185605-chr2:133187063..133189949,2	MCF-7	breast:
16	chr2:133124752..133127513-chr2:133337164..133339818,2	MCF-7	breast:
17	chr2:133184307..133187012-chr2:133200888..133203786,2	MCF-7	breast:
18	chr2:133340082..133340612-chr2:133355931..133356931,2	MCF-7	breast:
19	chr2:133136843..133139726-chr2:133171493..133174059,2	MCF-7	breast:
20	chr2:133339779..133340732-chr2:133641136..133642087,4	MCF-7	breast:
21	chr2:133174816..133177571-chr2:133199085..133201866,2	MCF-7	breast:
22	chr2:133174816..133177571-chr2:133199085..133201866,2	MCF-7	breast:
23	chr2:133228178..133229976-chr2:133230852..133233408,2	MCF-7	breast:
24	chr2:133274709..133277168-chr2:133277775..133280190,2	K562	blood:
25	chr2:133335745..133337645-chr2:133340420..133342351,2	K562	blood:
26	chr2:133340023..133340581-chr2:134469532..134470151,2	MCF-7	breast:
27	chr2:133184307..133187012-chr2:133200888..133203786,2	MCF-7	breast:
28	chr2:133218783..133221422-chr2:133221426..133223420,2	MCF-7	breast:
29	chr2:133312121..133314029-chr2:133316957..133319082,2	K562	blood:
30	chr2:133180532..133182214-chr2:133186789..133189602,2	MCF-7	breast:
31	chr2:133230048..133232279-chr2:133233399..133234934,2	MCF-7	breast:
32	chr2:133174198..133176133-chr2:133181878..133184436,2	MCF-7	breast:
33	chr2:133129464..133129981-chr2:133206123..133207082,2	MCF-7	breast:
34	chr2:133189109..133191436-chr2:133194344..133196000,2	MCF-7	breast:
35	chr2:133312121..133314029-chr2:133316957..133319082,2	K562	blood:
36	chr2:133308087..133308889-chr2:133339718..133340292,2	MCF-7	breast:
37	chr2:133164142..133169602-chr2:133170573..133175419,7	MCF-7	breast:
38	chr2:133180532..133182214-chr2:133186789..133189602,2	MCF-7	breast:
39	chr2:133304259..133305229-chr2:133647133..133647703,2	MCF-7	breast:
40	chr2:133174216..133177088-chr2:133183800..133185718,2	MCF-7	breast:
41	chr2:133340082..133340612-chr2:133355931..133356931,2	MCF-7	breast:
42	chr2:133104010..133106361-chr2:133176429..133178884,2	MCF-7	breast:
43	chr2:133108915..133111457-chr2:133172343..133174834,3	MCF-7	breast:
44	chr2:133173744..133175513-chr2:133427199..133429009,2	MCF-7	breast:
45	chr2:133195794..133199100-chr2:133203040..133205652,3	MCF-7	breast:
46	chr2:133339874..133340573-chr2:133634427..133635308,3	MCF-7	breast:
47	chr2:133171742..133175089-chr2:133186181..133188508,3	MCF-7	breast:
48	chr2:133195794..133199100-chr2:133203040..133205652,3	MCF-7	breast:
49	chr2:133189109..133191436-chr2:133194344..133196000,2	MCF-7	breast:
50	chr2:133339837..133340676-chr2:133369649..133370780,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf27A-10	chr2:133281190-133281509	NONHSAT074537
2	lnc-LYPD1-3	chr2:133246127-133246661	NONHSAT074536

No data

Variant related genes	Relation type
YBX1P7	TF binding region
GPR39	TF binding region
RNU6-175P	TF binding region
ENSG00000221142	TF binding region
RN7SKP103	TF binding region
YBX1P7	CpG island
GPR39	CpG island
RNU6-175P	CpG island
ENSG00000221142	CpG island
RN7SKP103	CpG island
ENSG00000272769	chromatin interactions
ENSG00000183840	chromatin interactions
ENSG00000252705	chromatin interactions
ENSG00000150551	chromatin interactions
ENSG00000221142	chromatin interactions
ENSG00000200718	chromatin interactions
ENSG00000230992	chromatin interactions

Extended variants
information (count: 7711 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:7711 , 50 per page) page: 1 2 3 4 5 6 7 ... 155

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10173228	chr2:133167263-133167264	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141157630	chr2:133167301-133167302	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181847634	chr2:133167302-133167303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531524709	chr2:133167319-133167320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544261389	chr2:133167395-133167396	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577825089	chr2:133167408-133167409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368981546	chr2:133167421-133167422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs72867731	chr2:133167465-133167466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564641125	chr2:133167469-133167470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34073169	chr2:133167484-133167485	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369408358	chr2:133167510-133167511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs528075877	chr2:133167525-133167526	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs547003187	chr2:133167529-133167530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs79519322	chr2:133167589-133167590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139018969	chr2:133167649-133167650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559483442	chr2:133167690-133167691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548846499	chr2:133167704-133167705	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142244892	chr2:133167714-133167715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545209531	chr2:133167737-133167738	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565004117	chr2:133167742-133167743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10173712	chr2:133167745-133167746	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559156322	chr2:133167752-133167753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566748174	chr2:133167774-133167775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577433095	chr2:133167811-133167812	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535095711	chr2:133167845-133167846	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs146377376	chr2:133167913-133167914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186338128	chr2:133167953-133167954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs6744134	chr2:133167978-133167979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542597596	chr2:133167988-133167989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs548942187	chr2:133167991-133167992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191088161	chr2:133168013-133168014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139351029	chr2:133168015-133168016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576210376	chr2:133168062-133168063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543222096	chr2:133168077-133168078	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564702963	chr2:133168193-133168194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182635517	chr2:133168200-133168201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550516089	chr2:133168216-133168217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs7582443	chr2:133168294-133168295	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537862485	chr2:133168392-133168393	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530321876	chr2:133168403-133168404	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529680238	chr2:133168423-133168424	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547014816	chr2:133168446-133168447	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548645379	chr2:133168457-133168458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570341257	chr2:133168496-133168497	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187596017	chr2:133168539-133168540	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373305769	chr2:133168577-133168578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34269262	chr2:133168599-133168600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531199547	chr2:133168607-133168608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4954322	chr2:133168623-133168624	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571036918	chr2:133168646-133168647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1573 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133164200-133173200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:133166000-133171000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:133166200-133169400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:133166400-133171200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr2:133166400-133171400	Weak transcription	Stomach Mucosa	stomach
6	chr2:133166400-133171600	Weak transcription	Pancreas	Pancrea
7	chr2:133166600-133171200	Weak transcription	Gastric	stomach
8	chr2:133166600-133171600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr2:133166800-133170800	Weak transcription	Fetal Intestine Large	intestine
10	chr2:133167000-133167400	Weak transcription	Fetal Intestine Small	intestine
11	chr2:133167400-133167600	Enhancers	Fetal Intestine Small	intestine
12	chr2:133167600-133171000	Weak transcription	Fetal Intestine Small	intestine
13	chr2:133169400-133169800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:133169600-133169800	Enhancers	A549	lung
15	chr2:133169800-133171800	Weak transcription	A549	lung
16	chr2:133170800-133173400	Enhancers	Fetal Intestine Large	intestine
17	chr2:133171000-133171200	Enhancers	Fetal Brain Female	brain
18	chr2:133171000-133171800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:133171000-133173200	Enhancers	Fetal Intestine Small	intestine
20	chr2:133171200-133171400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr2:133171200-133172000	Enhancers	Gastric	stomach
22	chr2:133171200-133172800	Weak transcription	Fetal Brain Female	brain
23	chr2:133171200-133173000	Enhancers	Duodenum Mucosa	Duodenum
24	chr2:133171200-133173400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:133171400-133173000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:133171400-133173000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr2:133171400-133173000	Enhancers	Stomach Mucosa	stomach
28	chr2:133171600-133171800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
29	chr2:133171600-133172000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr2:133171600-133172000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:133171600-133172000	Enhancers	Fetal Brain Male	brain
32	chr2:133171600-133172000	Enhancers	Pancreas	Pancrea
33	chr2:133171600-133172600	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr2:133171800-133172000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:133171800-133172000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:133171800-133172000	Bivalent Enhancer	Lung	lung
37	chr2:133171800-133172000	Flanking Bivalent TSS/Enh	Sigmoid Colon	Sigmoid Colon
38	chr2:133171800-133172200	Enhancers	NHDF-Ad	bronchial
39	chr2:133171800-133172600	Enhancers	A549	lung
40	chr2:133171800-133173000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:133171800-133173000	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr2:133171800-133173000	Enhancers	HSMMtube	muscle
43	chr2:133171800-133173200	Enhancers	NHLF	lung
44	chr2:133172000-133173000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:133172000-133173000	Weak transcription	Pancreas	Pancrea
46	chr2:133172000-133173200	Weak transcription	Fetal Brain Male	brain
47	chr2:133172000-133173200	Weak transcription	Gastric	stomach
48	chr2:133172200-133172600	Weak transcription	NHDF-Ad	bronchial
49	chr2:133172400-133173000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:133172400-133173000	Enhancers	Colonic Mucosa	Colon

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