Variant report

Variant	nsv522321
Chromosome Location	chr12:124383950-124424636
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:756)
CpG islands
(count:1344)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:756 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124395591-124395654	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:124397088-124397355	HepG2	liver:	n/a	n/a
3	ATF1	chr12:124404059-124404487	K562	blood:	n/a	n/a
4	ATF1	chr12:124419518-124419695	K562	blood:	n/a	n/a
5	ATF3	chr12:124385336-124385691	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr12:124385412-124385566	K562	blood:	n/a	n/a
7	BCL3	chr12:124401273-124401632	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:124423298-124423498	K562	blood:	n/a	n/a
9	BHLHE40	chr12:124404167-124404504	K562	blood:	n/a	n/a
10	BHLHE40	chr12:124416373-124416450	HepG2	liver:	n/a	n/a
11	BRCA1	chr12:124384821-124384855	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr12:124385316-124385710	K562	blood:	n/a	n/a
13	CEBPB	chr12:124411479-124411674	HepG2	liver:	n/a	chr12:124411536-124411547
14	CEBPB	chr12:124411383-124411696	IMR90	lung:	n/a	chr12:124411536-124411547
15	CEBPB	chr12:124389804-124390174	K562	blood:	n/a	chr12:124389984-124389995
16	CEBPB	chr12:124403958-124404449	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:124389800-124390188	Hela-S3	cervix:	n/a	chr12:124389984-124389995
18	CEBPB	chr12:124389682-124390301	A549	lung:	n/a	chr12:124389984-124389995
19	CEBPB	chr12:124423448-124423481	K562	blood:	n/a	n/a
20	CEBPB	chr12:124389848-124390167	ECC-1	luminal epithelium:	n/a	chr12:124389984-124389995
21	CEBPB	chr12:124389751-124390130	MCF-7	breast:	n/a	chr12:124389984-124389995
22	CEBPB	chr12:124392389-124392460	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:124389821-124390187	HepG2	liver:	n/a	chr12:124389984-124389995
24	CEBPB	chr12:124419517-124419665	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:124419497-124419700	K562	blood:	n/a	n/a
26	CEBPB	chr12:124389793-124390177	IMR90	lung:	n/a	chr12:124389984-124389995
27	CEBPB	chr12:124389816-124390173	A549	lung:	n/a	chr12:124389984-124389995
28	CEBPB	chr12:124419437-124419726	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:124389816-124390178	H1-hESC	embryonic stem cell:	n/a	chr12:124389984-124389995
30	CEBPB	chr12:124411400-124411578	K562	blood:	n/a	chr12:124411536-124411547
31	CEBPB	chr12:124389898-124390096	HepG2	liver:	n/a	chr12:124389984-124389995
32	CEBPB	chr12:124389783-124390267	MCF-7	breast:	n/a	chr12:124389984-124389995
33	CHD2	chr12:124385384-124385792	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr12:124395411-124395440	HepG2	liver:	n/a	n/a
35	CHD2	chr12:124423531-124423638	HepG2	liver:	n/a	n/a
36	CREB1	chr12:124404019-124404516	K562	blood:	n/a	n/a
37	CREB1	chr12:124404010-124404647	K562	blood:	n/a	n/a
38	CTCF	chr12:124423392-124423521	GM20000	blood:	n/a	n/a
39	CTCF	chr12:124423280-124423430	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr12:124418017-124418035	GM13976	blood:	n/a	n/a
41	CTCF	chr12:124423060-124423210	AG09309	skin:	n/a	chr12:124423095-124423103
42	CTCF	chr12:124423264-124423590	GM12878	blood:	n/a	n/a
43	CTCF	chr12:124390000-124390150	HAc	cerebellar:	n/a	n/a
44	CTCF	chr12:124423360-124423510	SAEC	small airway:	n/a	n/a
45	CTCF	chr12:124412900-124413050	GM12864	blood:	n/a	n/a
46	CTCF	chr12:124423360-124423510	GM12867	blood:	n/a	n/a
47	CTCF	chr12:124389600-124389750	HVMF	connective:	n/a	n/a
48	CTCF	chr12:124423401-124423483	GM13976	blood:	n/a	n/a
49	CTCF	chr12:124412940-124413090	GM12865	blood:	n/a	n/a
50	CTCF	chr12:124423300-124423450	GM12866	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124397892-124397942	GM12892	blood:	n/a
2	chr12:124419970-124420020	PANC-1	pancreas:	n/a
3	chr12:124397892-124397942	GM12892	blood:	n/a
4	chr12:124419970-124420020	PANC-1	pancreas:	n/a
5	chr12:124422061-124422111	BE2_C	brain:	n/a
6	chr12:124419970-124420020	AG10803	skin:	n/a
7	chr12:124392362-124392412	BE2_C	brain:	n/a
8	chr12:124393655-124393705	AG04450	lung:	fetal
9	chr12:124422135-124422185	Hepatocyte	liver:	n/a
10	chr12:124422061-124422111	HIPEpiC	eye:	n/a
11	chr12:124409762-124409812	SK-N-SH	brain:	n/a
12	chr12:124416206-124416256	HIPEpiC	eye:	n/a
13	chr12:124416315-124416365	PrEC	prostate:	n/a
14	chr12:124421953-124422003	SK-N-SH	brain:	n/a
15	chr12:124409684-124409734	NB4	blood:	n/a
16	chr12:124419970-124420020	HUVEC	blood vessel:	n/a
17	chr12:124393913-124393963	AG04450	lung:	fetal
18	chr12:124422061-124422111	BJ	skin:	n/a
19	chr12:124409762-124409812	PrEC	prostate:	n/a
20	chr12:124393655-124393705	ECC-1	luminal epithelium:	n/a
21	chr12:124392362-124392412	HCM	heart:	n/a
22	chr12:124393913-124393963	ovcar-3	ovarian:	n/a
23	chr12:124409762-124409812	HEEpiC	esophagus:	n/a
24	chr12:124422135-124422185	GM12892	blood:	n/a
25	chr12:124397892-124397942	Hela-S3	cervix:	n/a
26	chr12:124421953-124422003	GM12878	blood:	n/a
27	chr12:124422259-124422309	HCT-116	colon:	n/a
28	chr12:124393772-124393822	HNPCEpiC	eye:	n/a
29	chr12:124397892-124397942	ovcar-3	ovarian:	n/a
30	chr12:124421953-124422003	BJ	skin:	n/a
31	chr12:124392362-124392412	ProgFib	skin:	n/a
32	chr12:124393772-124393822	SK-N-MC	brain:	n/a
33	chr12:124388250-124388300	PFSK-1	brain:	n/a
34	chr12:124392362-124392412	GM12878	blood:	n/a
35	chr12:124397892-124397942	HEK293	kidney:	embryo
36	chr12:124421953-124422003	HRCEpiC	kidney:	n/a
37	chr12:124421582-124421632	HEEpiC	esophagus:	n/a
38	chr12:124409684-124409734	HRCEpiC	kidney:	n/a
39	chr12:124421382-124421432	NT2-D1	testis:	n/a
40	chr12:124416315-124416365	AoSMC	blood vessel:	n/a
41	chr12:124422259-124422309	NHDF-neo	bronchial:	n/a
42	chr12:124416206-124416256	CMK	blood:	n/a
43	chr12:124397810-124397860	PrEC	prostate:	n/a
44	chr12:124409804-124409854	HEEpiC	esophagus:	n/a
45	chr12:124409684-124409734	HCF	heart:	n/a
46	chr12:124422135-124422185	HCM	heart:	n/a
47	chr12:124424413-124424463	GM06990	blood:	n/a
48	chr12:124409684-124409734	AG04450	lung:	fetal
49	chr12:124422259-124422309	BE2_C	brain:	n/a
50	chr12:124419970-124420020	BJ	skin:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:124397721..124401102-chr12:124402433..124404220,3	K562	blood:
2	chr12:124409871..124412638-chr12:124416251..124418767,2	K562	blood:
3	chr12:124408910..124411445-chr12:124416040..124418769,2	MCF-7	breast:
4	chr12:124387569..124390026-chr12:124455814..124457883,2	MCF-7	breast:
5	chr12:124391978..124393581-chr12:124398813..124401282,2	MCF-7	breast:
6	chr12:124408910..124411445-chr12:124416040..124418769,2	MCF-7	breast:
7	chr12:124378198..124380132-chr12:124382297..124384260,2	K562	blood:
8	chr12:124397482..124399331-chr12:124424154..124425975,2	K562	blood:
9	chr12:124417812..124421208-chr12:124423467..124426187,5	MCF-7	breast:
10	chr12:124369425..124371891-chr12:124388110..124389965,2	MCF-7	breast:
11	chr12:124381734..124384108-chr12:124456893..124459517,2	MCF-7	breast:
12	chr12:124399326..124401527-chr12:124406576..124410878,3	MCF-7	breast:
13	chr12:124389600..124390517-chr12:124516534..124517510,2	K562	blood:
14	chr12:124397482..124399331-chr12:124424154..124425975,2	K562	blood:
15	chr12:124402948..124405033-chr12:124413350..124415168,2	MCF-7	breast:
16	chr12:124295197..124298095-chr12:124388889..124391568,2	MCF-7	breast:
17	chr12:124397721..124401102-chr12:124402433..124404220,3	K562	blood:
18	chr12:124402948..124405033-chr12:124413350..124415168,2	MCF-7	breast:
19	chr1:109583884..109584598-chr12:124392910..124393430,2	Hela-S3	cervix:
20	chr12:124377023..124380041-chr12:124383288..124384987,3	MCF-7	breast:
21	chr12:124389950..124393053-chr12:124455413..124457949,3	MCF-7	breast:
22	chr12:124389629..124391597-chr12:124394347..124396284,2	K562	blood:
23	chr12:124419434..124422110-chr12:124423989..124426076,2	K562	blood:
24	chr12:124407933..124410247-chr12:124410271..124413252,2	MCF-7	breast:
25	chr12:124389629..124391597-chr12:124394347..124396284,2	K562	blood:
26	chr12:124286094..124286683-chr12:124412581..124413486,2	MCF-7	breast:
27	chr12:124423442..124425248-chr12:124427955..124429927,2	MCF-7	breast:
28	chr12:124397207..124398875-chr12:124456168..124458505,2	MCF-7	breast:
29	chr12:124380887..124382932-chr12:124386966..124389727,2	K562	blood:
30	chr12:124407933..124410247-chr12:124410271..124413252,2	MCF-7	breast:
31	chr12:124379452..124381499-chr12:124383777..124386818,3	MCF-7	breast:
32	chr12:124419696..124421587-chr12:124455495..124458360,2	MCF-7	breast:
33	chr12:124409871..124412638-chr12:124416251..124418767,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAH10OS-1	chr12:124410008-124410630	ENSG00000270028.1
2	lnc-DNAH10OS-2	chr12:124420169-124420753	ENSG00000270005.1
3	lnc-CCDC92-1	chr12:124408539-124408835	NONHSAT031610

No data

Variant related genes	Relation type
ENSG00000270005	TF binding region
DNAH10	TF binding region
DNAH10OS	TF binding region
ENSG00000270028	TF binding region
ENSG00000270005	CpG island
DNAH10	CpG island
DNAH10OS	CpG island
ENSG00000270028	CpG island
ENSG00000270028	chromatin interactions
ENSG00000270095	chromatin interactions
ENSG00000178882	chromatin interactions
ENSG00000085433	chromatin interactions
ENSG00000179195	chromatin interactions
ENSG00000270005	chromatin interactions
ENSG00000119242	chromatin interactions
ENSG00000250091	chromatin interactions
ENSG00000197653	chromatin interactions

Extended variants
information (count: 1864 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1864 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10744163	chr12:124383950-124383951	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532906483	chr12:124384004-124384005	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551321399	chr12:124384010-124384011	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs190449708	chr12:124384019-124384020	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs540061801	chr12:124384037-124384038	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs374512883	chr12:124384052-124384053	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs114450792	chr12:124384074-124384075	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs151168093	chr12:124384130-124384131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146894439	chr12:124384142-124384143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs58278260	chr12:124384164-124384165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535186090	chr12:124384217-124384218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs180760946	chr12:124384323-124384324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs578026445	chr12:124384324-124384325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138955676	chr12:124384371-124384372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116615315	chr12:124384393-124384394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554637785	chr12:124384406-124384407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112961901	chr12:124384407-124384408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540219640	chr12:124384431-124384432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543699206	chr12:124384442-124384443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561688185	chr12:124384481-124384482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185327333	chr12:124384485-124384486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190083095	chr12:124384491-124384492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577437611	chr12:124384504-124384505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559137972	chr12:124384524-124384525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7294576	chr12:124384562-124384563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181411973	chr12:124384567-124384568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563292028	chr12:124384577-124384578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs201677652	chr12:124384626-124384627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549005276	chr12:124384640-124384641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559983940	chr12:124384649-124384650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35251089	chr12:124384711-124384712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546491929	chr12:124384739-124384740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186086219	chr12:124384746-124384747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563336878	chr12:124384753-124384754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143031303	chr12:124384763-124384764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145614184	chr12:124384769-124384770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539103823	chr12:124384810-124384811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557221019	chr12:124384824-124384825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575585329	chr12:124384838-124384839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544045934	chr12:124384874-124384875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148216971	chr12:124384904-124384905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79298571	chr12:124384925-124384926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531919513	chr12:124384942-124384943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368788634	chr12:124384953-124384954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78477816	chr12:124384967-124384968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192002569	chr12:124385009-124385010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577807043	chr12:124385042-124385043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs10846574	chr12:124385058-124385059	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563192608	chr12:124385071-124385072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530630776	chr12:124385072-124385073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124380000-124385600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr12:124381800-124384000	Weak transcription	Fetal Brain Male	brain
3	chr12:124382000-124385400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr12:124382000-124391400	Weak transcription	Fetal Lung	lung
5	chr12:124382200-124385400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr12:124383800-124384000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr12:124383800-124384000	Enhancers	Right Ventricle	heart
8	chr12:124384000-124384200	Enhancers	Fetal Brain Male	brain
9	chr12:124384000-124384200	Enhancers	Spleen	Spleen
10	chr12:124384000-124408400	Weak transcription	Fetal Brain Female	brain
11	chr12:124384200-124387000	Weak transcription	Spleen	Spleen
12	chr12:124385000-124387200	Enhancers	Fetal Thymus	thymus
13	chr12:124385200-124386000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr12:124385200-124386200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:124385200-124386200	Enhancers	Thymus	Thymus
16	chr12:124385400-124385600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr12:124385400-124385800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:124385400-124386000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr12:124385400-124386200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:124385400-124386200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr12:124385400-124386200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr12:124385400-124386200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:124385400-124386200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:124385400-124386200	Enhancers	Primary hematopoietic stem cells	blood
25	chr12:124385400-124386200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr12:124385400-124386200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:124385400-124386800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:124385400-124386800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr12:124385400-124390200	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr12:124385600-124385800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr12:124385600-124385800	Enhancers	Right Ventricle	heart
32	chr12:124385600-124386000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr12:124385600-124386000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:124385600-124386000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr12:124385600-124386000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr12:124385600-124386000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
37	chr12:124385600-124386000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
38	chr12:124385600-124386000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:124385600-124386000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr12:124385600-124386000	Bivalent Enhancer	Placenta	Placenta
41	chr12:124385600-124386000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr12:124385600-124386000	Bivalent/Poised TSS	HepG2	liver
43	chr12:124385600-124386200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr12:124385600-124386200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:124385600-124386200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr12:124385600-124386200	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:124385600-124386200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr12:124385600-124386200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr12:124385600-124386200	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr12:124385800-124386000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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