Variant report

Variant	nsv915754
Chromosome Location	chr12:34052409-34756196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4203)
CpG islands
(count:12159)
Chromatin interactive
region (count:87)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4203 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:34174965-34175535	K562	blood:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
2	ARID3A	chr12:34417095-34417295	K562	blood:	n/a	n/a
3	ARID3A	chr12:34174917-34175527	HepG2	liver:	n/a	chr12:34175026-34175042 chr12:34175027-34175043
4	ARID3A	chr12:34372445-34372838	K562	blood:	n/a	n/a
5	ARID3A	chr12:34186859-34187191	K562	blood:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
6	ARID3A	chr12:34367118-34367148	K562	blood:	n/a	n/a
7	ARID3A	chr12:34098056-34098330	HepG2	liver:	n/a	n/a
8	ARID3A	chr12:34276078-34276334	K562	blood:	n/a	n/a
9	ARID3A	chr12:34186930-34187207	HepG2	liver:	n/a	chr12:34187070-34187086 chr12:34187069-34187085
10	ARID3A	chr12:34276092-34276305	HepG2	liver:	n/a	n/a
11	ATF1	chr12:34276078-34276281	K562	blood:	n/a	n/a
12	ATF1	chr12:34407159-34407233	K562	blood:	n/a	n/a
13	ATF1	chr12:34175112-34175525	K562	blood:	n/a	n/a
14	ATF1	chr12:34372443-34372838	K562	blood:	n/a	n/a
15	ATF1	chr12:34340026-34340130	K562	blood:	n/a	n/a
16	ATF1	chr12:34250260-34250470	K562	blood:	n/a	n/a
17	ATF1	chr12:34280414-34280639	K562	blood:	n/a	n/a
18	ATF1	chr12:34430831-34430993	K562	blood:	n/a	n/a
19	ATF2	chr12:34175128-34175510	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr12:34175036-34175597	GM12878	blood:	n/a	n/a
21	ATF2	chr12:34174909-34175573	GM12878	blood:	n/a	n/a
22	ATF2	chr12:34175155-34175514	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr12:34280320-34280675	K562	blood:	n/a	n/a
24	ATF3	chr12:34175027-34175625	A549	lung:	n/a	n/a
25	ATF3	chr12:34372504-34372902	A549	lung:	n/a	n/a
26	ATF3	chr12:34275984-34276254	GM12878	blood:	n/a	n/a
27	ATF3	chr12:34372398-34372788	A549	lung:	n/a	n/a
28	ATF3	chr12:34509280-34509455	K562	blood:	n/a	n/a
29	ATF3	chr12:34509237-34509520	K562	blood:	n/a	n/a
30	ATF3	chr12:34175051-34175608	A549	lung:	n/a	n/a
31	BACH1	chr12:34429857-34430227	K562	blood:	n/a	n/a
32	BACH1	chr12:34486593-34486711	K562	blood:	n/a	n/a
33	BACH1	chr12:34186563-34186928	H1-hESC	embryonic stem cell:	n/a	chr12:34186742-34186756
34	BACH1	chr12:34489607-34489683	K562	blood:	n/a	n/a
35	BACH1	chr12:34500299-34500489	K562	blood:	n/a	n/a
36	BACH1	chr12:34429537-34429559	K562	blood:	n/a	n/a
37	BACH1	chr12:34369832-34370042	K562	blood:	n/a	n/a
38	BACH1	chr12:34428886-34428914	K562	blood:	n/a	n/a
39	BACH1	chr12:34417075-34417361	K562	blood:	n/a	n/a
40	BACH1	chr12:34417965-34418172	K562	blood:	n/a	n/a
41	BACH1	chr12:34186566-34186928	K562	blood:	n/a	chr12:34186742-34186756
42	BATF	chr12:34387277-34387522	GM12878	blood:	n/a	n/a
43	BATF	chr12:34374801-34375081	GM12878	blood:	n/a	n/a
44	BATF	chr12:34207885-34208102	GM12878	blood:	n/a	n/a
45	BATF	chr12:34279173-34279432	GM12878	blood:	n/a	n/a
46	BATF	chr12:34175171-34175544	GM12878	blood:	n/a	n/a
47	BATF	chr12:34207658-34207839	GM12878	blood:	n/a	n/a
48	BATF	chr12:34372475-34372720	GM12878	blood:	n/a	n/a
49	BATF	chr12:34575259-34575544	GM12878	blood:	n/a	n/a
50	BATF	chr12:34575360-34575508	GM12878	blood:	n/a	n/a

(count:12159 , 50 per page) page: 1 2 3 4 5 6 7 ... 244

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34445809-34445859	Hela-S3	cervix:	n/a
2	chr12:34443659-34443709	GM12891	blood:	n/a
3	chr12:34556037-34556087	A549	lung:	n/a
4	chr12:34318527-34318577	HCM	heart:	n/a
5	chr12:34755315-34755365	MCF10A-Er-Src	breast:	n/a
6	chr12:34488920-34488970	NH-A	brain:	n/a
7	chr12:34527230-34527280	CMK	blood:	n/a
8	chr12:34546775-34546825	Caco-2	colon:	n/a
9	chr12:34551994-34552044	NH-A	brain:	n/a
10	chr12:34471040-34471090	H1-hESC	embryonic stem cell:	embryo
11	chr12:34491090-34491140	GM12891	blood:	n/a
12	chr12:34754948-34754998	HepG2	liver:	n/a
13	chr12:34500640-34500690	GM19239	blood:	n/a
14	chr12:34372299-34372349	GM19239	blood:	n/a
15	chr12:34491090-34491140	GM06990	blood:	n/a
16	chr12:34554731-34554781	U87	brain:	n/a
17	chr12:34551489-34551539	HCPEpiC	choroid plexus:	n/a
18	chr12:34488920-34488970	HUVEC	blood vessel:	n/a
19	chr12:34548094-34548144	ovcar-3	ovarian:	n/a
20	chr12:34441774-34441824	HRPEpiC	eye:	n/a
21	chr12:34445809-34445859	Hela-S3	cervix:	n/a
22	chr12:34443659-34443709	GM12891	blood:	n/a
23	chr12:34556037-34556087	A549	lung:	n/a
24	chr12:34318527-34318577	HCM	heart:	n/a
25	chr12:34755315-34755365	MCF10A-Er-Src	breast:	n/a
26	chr12:34488920-34488970	NH-A	brain:	n/a
27	chr12:34527230-34527280	CMK	blood:	n/a
28	chr12:34546775-34546825	Caco-2	colon:	n/a
29	chr12:34551994-34552044	NH-A	brain:	n/a
30	chr12:34471040-34471090	H1-hESC	embryonic stem cell:	embryo
31	chr12:34491090-34491140	GM12891	blood:	n/a
32	chr12:34754948-34754998	HepG2	liver:	n/a
33	chr12:34500640-34500690	GM19239	blood:	n/a
34	chr12:34372299-34372349	GM19239	blood:	n/a
35	chr12:34491090-34491140	GM06990	blood:	n/a
36	chr12:34554731-34554781	U87	brain:	n/a
37	chr12:34551489-34551539	HCPEpiC	choroid plexus:	n/a
38	chr12:34488920-34488970	HUVEC	blood vessel:	n/a
39	chr12:34548094-34548144	ovcar-3	ovarian:	n/a
40	chr12:34441774-34441824	HRPEpiC	eye:	n/a
41	chr12:34537250-34537300	NB4	blood:	n/a
42	chr12:34442705-34442755	SK-N-MC	brain:	n/a
43	chr12:34500585-34500635	HMEC	breast:	n/a
44	chr12:34516072-34516122	HUVEC	blood vessel:	n/a
45	chr12:34061681-34061731	HAEpiC	amniotic membrane:	n/a
46	chr12:34532907-34532957	HMEC	breast:	n/a
47	chr12:34495509-34495559	GM12891	blood:	n/a
48	chr12:34519837-34519887	RPTEC	kidney:	n/a
49	chr12:34319740-34319790	HNPCEpiC	eye:	n/a
50	chr12:34489827-34489877	HCM	heart:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:34372145..34372649-chr9:79186173..79186679,2	MCF-7	breast:
2	chr12:34427757..34428277-chr16:33958747..33959470,2	MCF-7	breast:
3	chr1:91852330..91853034-chr12:34372628..34373167,11	MCF-7	breast:
4	chr12:34544160..34546005-chr12:34547460..34549884,2	K562	blood:
5	chr12:34275751..34276656-chr12:34370666..34371823,3	MCF-7	breast:
6	chr12:34277684..34281105-chr12:34367413..34370316,3	K562	blood:
7	chr12:34191233..34191868-chr12:34777963..34778741,2	MCF-7	breast:
8	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
9	chr12:34497610..34503522-chr12:34523490..34528831,5	K562	blood:
10	chr12:34275785..34276629-chr12:34339119..34339912,4	MCF-7	breast:
11	chr12:34513093..34516192-chr12:34527570..34530403,3	K562	blood:
12	chr12:34497610..34503522-chr12:34523490..34528831,5	K562	blood:
13	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
14	chr12:32908405..32909605-chr12:34174701..34175708,3	MCF-7	breast:
15	chr12:34542219..34546005-chr12:34547286..34550175,4	K562	blood:
16	chr1:91851338..91852967-chr12:34372628..34374131,2	K562	blood:
17	chr12:34276079..34276686-chr12:34371078..34371813,4	MCF-7	breast:
18	chr12:34275679..34276702-chr12:34339057..34340086,5	MCF-7	breast:
19	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
20	chr12:34543477..34545374-chr12:34550348..34552407,2	K562	blood:
21	chr12:34097991..34100054-chr12:60091596..60093323,2	MCF-7	breast:
22	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
23	chr1:91852303..91852973-chr12:34372638..34373146,2	HCT-116	colon:
24	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
25	chr12:34275776..34276287-chr12:34445928..34446780,2	MCF-7	breast:
26	chr12:34277684..34280343-chr12:34367543..34370316,2	K562	blood:
27	chr12:34497129..34499259-chr12:34508235..34509796,2	K562	blood:
28	chr12:34487742..34489883-chr12:34492282..34495193,2	K562	blood:
29	chr12:34145843..34147953-chr17:56709056..56711203,2	MCF-7	breast:
30	chr12:34497467..34501951-chr12:34506676..34509735,4	K562	blood:
31	chr12:34480099..34482680-chr12:34485043..34486658,2	K562	blood:
32	chr1:91852282..91853087-chr12:34372625..34373157,6	MCF-7	breast:
33	chr12:34098748..34102292-chr12:49653830..49659564,5	MCF-7	breast:
34	chr1:91851344..91853074-chr12:34372634..34374167,5	MCF-7	breast:
35	chr12:34053367..34054987-chr12:34055066..34057564,2	MCF-7	breast:
36	chr12:32905758..32908162-chr12:34183695..34185541,2	K562	blood:
37	chr12:34372136..34372665-chr12:127650606..127651138,2	MCF-7	breast:
38	chr12:34472451..34474607-chr12:34482688..34484610,2	K562	blood:
39	chr12:34098184..34100062-chr12:60091369..60093533,4	MCF-7	breast:
40	chr12:34279057..34280887-chr12:34440053..34441876,2	K562	blood:
41	chr12:34491491..34493706-chr12:34544208..34545803,2	K562	blood:
42	chr1:91852355..91852916-chr12:34372634..34373168,4	MCF-7	breast:
43	chr12:34241238..34243550-chr12:38853316..38855678,2	MCF-7	breast:
44	chr12:34277684..34281105-chr12:34367413..34370316,3	K562	blood:
45	chr12:34543477..34545374-chr12:34550348..34552407,2	K562	blood:
46	chr12:34405769..34407368-chr12:38464924..38466718,2	K562	blood:
47	chr12:34159858..34162837-chr12:34175347..34177852,2	K562	blood:
48	chr12:34275803..34276751-chr12:34446099..34446740,3	K562	blood:
49	chr12:34247375..34249864-chr12:34256794..34259523,2	MCF-7	breast:
50	chr1:91851334..91853102-chr12:34372625..34374158,7	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-5	chr12:34421984-34422141	NONHSAT027661
2	lnc-ALG10-2	chr12:34315112-34315173	ENSG00000255628
3	lnc-ALG10-3	chr12:34315397-34315903	NONHSAT027653
4	lnc-ALG10-1	chr12:34190307-34190583	XLOC_009707
5	lnc-ALG10-1	chr12:34208992-34209394	XLOC_009707
6	lnc-ALG10-1	chr12:34208992-34209394	ENSG00000256538
7	lnc-ALG10-1	chr12:34190373-34190583	ENSG00000256538
8	lnc-ALG10-2	chr12:34302774-34303105	ENSG00000255628
9	lnc-ALG10-4	chr12:34402416-34402893	NONHSAT140067
10	lnc-ALG10-1	chr12:34209496-34209704	XLOC_009707
11	lnc-ALG10-2	chr12:34309116-34309255	ENSG00000255628
12	lnc-ALG10-5	chr12:34430929-34431017	NONHSAT027661
13	lnc-ALG10-1	chr12:34209496-34209675	ENSG00000256538

No data

Variant related genes	Relation type
ALG10	TF binding region
ENSG00000245482	TF binding region
ENSG00000201624	TF binding region
ENSG00000264446	TF binding region
ENSG00000255652	TF binding region
ENSG00000256986	TF binding region
TUBB8P4	TF binding region
ENSG00000256614	TF binding region
ENSG00000255628	TF binding region
ENSG00000256538	TF binding region
ENSG00000272435	TF binding region
RNU6-472P	TF binding region
ENSG00000258794	TF binding region
ALG10	CpG island
ENSG00000245482	CpG island
ENSG00000201624	CpG island
ENSG00000264446	CpG island
ENSG00000255652	CpG island
ENSG00000256986	CpG island
TUBB8P4	CpG island
ENSG00000256614	CpG island
ENSG00000255628	CpG island
ENSG00000256538	CpG island
ENSG00000272435	CpG island
RNU6-472P	CpG island
ENSG00000258794	CpG island
ENSG00000241781	chromatin interactions
ENSG00000175548	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000255652	chromatin interactions
ENSG00000239776	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000139133	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000226958	chromatin interactions
ENSG00000212195	chromatin interactions
PPARGC1A	miRNA target sites

Extended variants
information (count: 27969 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:27969 , 50 per page) page: 1 2 3 4 5 6 7 ... 560

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527287660	chr12:34060426-34060427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs16921376	chr12:34060436-34060437	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548124695	chr12:34060440-34060441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566666277	chr12:34060463-34060464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530210078	chr12:34060537-34060538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs550384211	chr12:34060543-34060544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs202000091	chr12:34060559-34060560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs16921377	chr12:34060616-34060617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545692888	chr12:34060636-34060637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532684229	chr12:34060682-34060683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552255304	chr12:34060690-34060691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565692983	chr12:34060722-34060723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534709535	chr12:34060725-34060726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563695543	chr12:34060734-34060735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35080890	chr12:34060797-34060798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187937316	chr12:34060831-34060832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567582769	chr12:34060843-34060844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536045898	chr12:34060887-34060888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556365956	chr12:34060909-34060910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528066356	chr12:34060943-34060944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577999823	chr12:34061013-34061014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs397850554	chr12:34061027-34061028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs33913747	chr12:34061028-34061029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558250699	chr12:34061033-34061034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2636089	chr12:34061091-34061092	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs572036920	chr12:34061098-34061099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73101262	chr12:34061178-34061179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs561549953	chr12:34061229-34061230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546324030	chr12:34061247-34061248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530463928	chr12:34061257-34061258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191238833	chr12:34061260-34061261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563857112	chr12:34061269-34061270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532605445	chr12:34061271-34061272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4143174	chr12:34061277-34061278	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs200475543	chr12:34061320-34061321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182232151	chr12:34061322-34061323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528448291	chr12:34061372-34061373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548215040	chr12:34061380-34061381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4143173	chr12:34061383-34061384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186836512	chr12:34061386-34061387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150351618	chr12:34061397-34061398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192749610	chr12:34061433-34061434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11052992	chr12:34061556-34061557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs144119001	chr12:34061560-34061561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3884210	chr12:34061561-34061562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112390580	chr12:34061567-34061568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142709166	chr12:34061587-34061588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73101263	chr12:34061592-34061593	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs80202296	chr12:34061605-34061606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374332415	chr12:34061618-34061619	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Bipolar disorder	19214233	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34060400-34063400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr12:34061200-34062800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:34061200-34062800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:34061400-34062800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:34061400-34062800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr12:34061400-34063400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:34061600-34062600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:34061800-34062000	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr12:34061800-34062800	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr12:34062000-34062400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr12:34062000-34062800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr12:34062400-34062600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:34062800-34067600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:34067600-34068000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr12:34067600-34068000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr12:34090000-34090400	Enhancers	Liver	Liver
17	chr12:34090400-34090800	Weak transcription	Liver	Liver
18	chr12:34090800-34092000	Enhancers	Liver	Liver
19	chr12:34092000-34096800	Weak transcription	Liver	Liver
20	chr12:34093800-34130400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:34096800-34098000	Enhancers	HMEC	breast
22	chr12:34096800-34098200	Enhancers	Liver	Liver
23	chr12:34097800-34098200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:34097800-34098400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr12:34098200-34098600	Flanking Active TSS	Liver	Liver
26	chr12:34098600-34098800	Enhancers	Liver	Liver
27	chr12:34099800-34100000	ZNF genes & repeats	Psoas Muscle	Psoas
28	chr12:34120200-34120800	Enhancers	HMEC	breast
29	chr12:34120400-34120800	Enhancers	NHEK	skin
30	chr12:34127800-34128000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:34130400-34130800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:34130800-34141200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:34131200-34131800	Enhancers	Liver	Liver
34	chr12:34140600-34142000	Enhancers	HMEC	breast
35	chr12:34141000-34142400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:34141000-34142800	Enhancers	NHEK	skin
37	chr12:34141200-34142000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:34141400-34142000	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr12:34141800-34142600	Enhancers	HUVEC	blood vessel
40	chr12:34141800-34142800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:34142000-34142800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:34142000-34146800	Weak transcription	HMEC	breast
43	chr12:34142000-34147200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:34142400-34147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:34142800-34143000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr12:34142800-34147400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:34142800-34147400	Weak transcription	NHEK	skin
48	chr12:34143000-34149600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:34146800-34148400	Enhancers	HMEC	breast
50	chr12:34147200-34148800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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