Variant report

Variant	nsv899282
Chromosome Location	chr12:74315252-74505531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:791)
CpG islands
(count:184)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:791 , 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	chr12:74415614-74416259	K562	blood:	n/a	n/a
2	ARID3A	chr12:74437204-74437450	K562	blood:	n/a	n/a
3	ARID3A	chr12:74416890-74416941	K562	blood:	n/a	n/a
4	ATF1	chr12:74505524-74505833	K562	blood:	n/a	n/a
5	ATF1	chr12:74415634-74416199	K562	blood:	n/a	n/a
6	ATF1	chr12:74433064-74433212	K562	blood:	n/a	n/a
7	ATF3	chr12:74415536-74416125	A549	lung:	n/a	n/a
8	ATF3	chr12:74436987-74437740	A549	lung:	n/a	n/a
9	ATF3	chr12:74415787-74416157	K562	blood:	n/a	n/a
10	BACH1	chr12:74437098-74437429	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:74436693-74436701	K562	blood:	n/a	n/a
12	BACH1	chr12:74437237-74437436	K562	blood:	n/a	n/a
13	BACH1	chr12:74354623-74354751	K562	blood:	n/a	n/a
14	BCL3	chr12:74436864-74437725	A549	lung:	n/a	n/a
15	BHLHE40	chr12:74415667-74416150	K562	blood:	n/a	n/a
16	BHLHE40	chr12:74402950-74402962	K562	blood:	n/a	n/a
17	BRCA1	chr12:74434492-74434514	GM12878	blood:	n/a	n/a
18	BRCA1	chr12:74382302-74382380	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr12:74415647-74416021	K562	blood:	n/a	n/a
20	CBX3	chr12:74436945-74437658	HCT-116	colon:	n/a	n/a
21	CBX3	chr12:74415640-74416084	K562	blood:	n/a	n/a
22	CBX3	chr12:74436882-74437716	HCT-116	colon:	n/a	n/a
23	CBX3	chr12:74505433-74505896	HCT-116	colon:	n/a	n/a
24	CCNT2	chr12:74415757-74416216	K562	blood:	n/a	n/a
25	CEBPB	chr12:74355992-74356257	HepG2	liver:	n/a	chr12:74356100-74356111
26	CEBPB	chr12:74415688-74416147	A549	lung:	n/a	n/a
27	CEBPB	chr12:74415769-74416185	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:74401087-74401214	A549	lung:	n/a	n/a
29	CEBPB	chr12:74333490-74333716	HepG2	liver:	n/a	chr12:74333596-74333607
30	CEBPB	chr12:74400232-74400470	HepG2	liver:	n/a	chr12:74400328-74400339
31	CEBPB	chr12:74436955-74437818	A549	lung:	n/a	n/a
32	CEBPB	chr12:74328114-74328196	HepG2	liver:	n/a	chr12:74328137-74328148 chr12:74328137-74328150 chr12:74328138-74328149
33	CEBPB	chr12:74437025-74437712	MCF-7	breast:	n/a	n/a
34	CEBPB	chr12:74437045-74437671	A549	lung:	n/a	n/a
35	CEBPB	chr12:74398911-74399207	K562	blood:	n/a	n/a
36	CEBPB	chr12:74354525-74354712	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:74398796-74399307	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:74356715-74356913	HepG2	liver:	n/a	chr12:74356844-74356855 chr12:74356844-74356857 chr12:74356845-74356856 chr12:74356844-74356857
39	CEBPB	chr12:74352692-74352867	A549	lung:	n/a	chr12:74352726-74352737
40	CEBPB	chr12:74444888-74445088	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr12:74399081-74399271	A549	lung:	n/a	n/a
42	CEBPB	chr12:74415929-74416125	K562	blood:	n/a	n/a
43	CEBPB	chr12:74456800-74457031	A549	lung:	n/a	chr12:74456926-74456937
44	CEBPB	chr12:74415768-74416234	K562	blood:	n/a	n/a
45	CEBPB	chr12:74415624-74416265	K562	blood:	n/a	n/a
46	CEBPB	chr12:74505523-74505779	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr12:74340620-74340772	HepG2	liver:	n/a	chr12:74340726-74340737
48	CEBPB	chr12:74328118-74328249	A549	lung:	n/a	chr12:74328137-74328148 chr12:74328137-74328150 chr12:74328138-74328149
49	CEBPB	chr12:74456774-74456982	HepG2	liver:	n/a	chr12:74456926-74456937
50	CEBPB	chr12:74445592-74445973	H1-hESC	embryonic stem cell:	n/a	chr12:74445783-74445794 chr12:74445783-74445794

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74442868-74442918	RPTEC	kidney:	n/a
2	chr12:74442868-74442918	RPTEC	kidney:	n/a
3	chr12:74431418-74431468	HL-60	blood:	n/a
4	chr12:74442868-74442918	T-47D	breast:	n/a
5	chr12:74444245-74444295	AoSMC	blood vessel:	n/a
6	chr12:74431418-74431468	ECC-1	luminal epithelium:	n/a
7	chr12:74442868-74442918	BJ	skin:	n/a
8	chr12:74442868-74442918	SK-N-SH_RA	brain:	n/a
9	chr12:74442868-74442918	IMR90	lung:	fetal
10	chr12:74444245-74444295	GM12891	blood:	n/a
11	chr12:74444245-74444295	HCM	heart:	n/a
12	chr12:74442868-74442918	HCM	heart:	n/a
13	chr12:74444245-74444295	SKMC	muscle:	n/a
14	chr12:74442868-74442918	ovcar-3	ovarian:	n/a
15	chr12:74444245-74444295	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:74431418-74431468	A549	lung:	n/a
17	chr12:74431418-74431468	NHBE	bronchial:	n/a
18	chr12:74442868-74442918	AoSMC	blood vessel:	n/a
19	chr12:74444245-74444295	H1-hESC	embryonic stem cell:	embryo
20	chr12:74442868-74442918	NT2-D1	testis:	n/a
21	chr12:74442868-74442918	HCPEpiC	choroid plexus:	n/a
22	chr12:74431418-74431468	Hepatocyte	liver:	n/a
23	chr12:74444245-74444295	HEEpiC	esophagus:	n/a
24	chr12:74431418-74431468	CMK	blood:	n/a
25	chr12:74442868-74442918	AG09319	gingival:	n/a
26	chr12:74442868-74442918	GM12891	blood:	n/a
27	chr12:74444245-74444295	HIPEpiC	eye:	n/a
28	chr12:74431418-74431468	GM19239	blood:	n/a
29	chr12:74431418-74431468	Caco-2	colon:	n/a
30	chr12:74431418-74431468	IMR90	lung:	fetal
31	chr12:74444245-74444295	K562	blood:	n/a
32	chr12:74444245-74444295	AG04450	lung:	fetal
33	chr12:74444245-74444295	PANC-1	pancreas:	n/a
34	chr12:74431418-74431468	ovcar-3	ovarian:	n/a
35	chr12:74444245-74444295	Hela-S3	cervix:	n/a
36	chr12:74431418-74431468	SKMC	muscle:	n/a
37	chr12:74442868-74442918	HRCEpiC	kidney:	n/a
38	chr12:74442868-74442918	PFSK-1	brain:	n/a
39	chr12:74444245-74444295	GM06990	blood:	n/a
40	chr12:74444245-74444295	HNPCEpiC	eye:	n/a
41	chr12:74444245-74444295	AG09319	gingival:	n/a
42	chr12:74444245-74444295	ovcar-3	ovarian:	n/a
43	chr12:74431418-74431468	NH-A	brain:	n/a
44	chr12:74431418-74431468	HIPEpiC	eye:	n/a
45	chr12:74442868-74442918	AG10803	skin:	n/a
46	chr12:74431418-74431468	BJ	skin:	n/a
47	chr12:74442868-74442918	AG09309	skin:	n/a
48	chr12:74431418-74431468	HEEpiC	esophagus:	n/a
49	chr12:74444245-74444295	SK-N-SH	brain:	n/a
50	chr12:74442868-74442918	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:74421024..74423356-chr12:74425327..74427373,2	K562	blood:
2	chr12:74505239..74506034-chr12:74759124..74759988,3	MCF-7	breast:
3	chr12:74447256..74448968-chr12:74473500..74476491,2	MCF-7	breast:
4	chr12:74491549..74494531-chr12:74496083..74497929,2	K562	blood:
5	chr12:74489819..74492327-chr12:74494030..74495535,2	K562	blood:
6	chr12:74505235..74505774-chr12:74710528..74711393,3	K562	blood:
7	chr12:74338246..74340293-chr17:57922225..57924227,2	MCF-7	breast:
8	chr12:74415389..74416204-chr12:74806037..74807059,3	MCF-7	breast:
9	chr12:74326236..74328077-chr12:74328827..74331756,2	K562	blood:
10	chr12:74294795..74296655-chr12:74314771..74316525,2	K562	blood:
11	chr12:74443201..74445435-chr12:74461454..74463551,2	MCF-7	breast:
12	chr12:74421024..74423356-chr12:74425327..74427373,2	K562	blood:
13	chr12:74412851..74416125-chr12:74417786..74420927,4	MCF-7	breast:
14	chr12:74417711..74420682-chr12:74422283..74426238,3	K562	blood:
15	chr12:74489819..74492327-chr12:74494030..74495535,2	K562	blood:
16	chr12:74415312..74416230-chr12:74710631..74711359,2	MCF-7	breast:
17	chr12:74439944..74442321-chr12:74443241..74445352,2	MCF-7	breast:
18	chr12:74415701..74416228-chr12:74504378..74504925,2	MCF-7	breast:
19	chr12:74443201..74445435-chr12:74461454..74463551,2	MCF-7	breast:
20	chr12:74326236..74328077-chr12:74328827..74331756,2	K562	blood:
21	chr12:74439944..74442321-chr12:74443241..74445352,2	MCF-7	breast:
22	chr12:74415701..74416228-chr12:74504378..74504925,2	MCF-7	breast:
23	chr12:74417711..74420682-chr12:74422283..74426238,3	K562	blood:
24	chr12:74389722..74391980-chr12:74584509..74586133,2	K562	blood:
25	chr12:74406595..74409366-chr12:74411193..74413349,2	MCF-7	breast:
26	chr12:74329268..74329785-chr12:74806142..74806934,2	K562	blood:
27	chr12:74415229..74416317-chr12:74501474..74502787,6	MCF-7	breast:
28	chr12:74415229..74416317-chr12:74501474..74502787,6	MCF-7	breast:
29	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
30	chr12:74491549..74494531-chr12:74496083..74497929,2	K562	blood:
31	chr12:74412851..74416125-chr12:74417786..74420927,4	MCF-7	breast:
32	chr12:74415343..74416036-chr12:74759116..74760027,3	MCF-7	breast:
33	chr12:74447256..74448968-chr12:74473500..74476491,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-4	chr12:74335897-74335956	ENSG00000258109
2	lnc-ATXN7L3B-1	chr12:74439438-74439608	ENSG00000258332
3	lnc-ATXN7L3B-1	chr12:74432866-74433237	ENSG00000258332

No data

Variant related genes	Relation type
ENSG00000258332	TF binding region
ENSG00000264155	TF binding region
ENSG00000258332	CpG island
ENSG00000264155	CpG island
ENSG00000264155	chromatin interactions
ZNF148	miRNA target sites
PLXNB2	miRNA target sites
TRIM2	miRNA target sites

Extended variants
information (count: 1376 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1376 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111979212	chr12:74326009-74326010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557399092	chr12:74326052-74326053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574165283	chr12:74326090-74326091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192295107	chr12:74326136-74326137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559797683	chr12:74326194-74326195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184661319	chr12:74326211-74326212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541069952	chr12:74326214-74326215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564057965	chr12:74326239-74326240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146037965	chr12:74326301-74326302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549744140	chr12:74332418-74332419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181446622	chr12:74332419-74332420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576183537	chr12:74332460-74332461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34922321	chr12:74332498-74332499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs534259583	chr12:74332523-74332524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529028674	chr12:74332537-74332538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548882623	chr12:74332543-74332544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141633939	chr12:74332561-74332562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547304215	chr12:74339050-74339051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564326578	chr12:74339085-74339086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562712304	chr12:74339106-74339107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144541058	chr12:74339176-74339177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569569596	chr12:74339182-74339183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535504468	chr12:74339187-74339188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548958463	chr12:74339277-74339278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7311068	chr12:74339372-74339373	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs535098410	chr12:74339399-74339400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376717942	chr12:74339410-74339411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557945518	chr12:74339451-74339452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs578128857	chr12:74339461-74339462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537592785	chr12:74339471-74339472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570977438	chr12:74339502-74339503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146148565	chr12:74339508-74339509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs140032660	chr12:74339524-74339525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143559100	chr12:74339567-74339568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541988735	chr12:74339607-74339608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541137554	chr12:74339610-74339611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563985112	chr12:74339611-74339612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371324789	chr12:74339629-74339630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549221006	chr12:74339678-74339679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533155987	chr12:74339688-74339689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145763832	chr12:74339752-74339753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563285672	chr12:74339821-74339822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529137860	chr12:74339838-74339839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10879712	chr12:74339853-74339854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs561686127	chr12:74339891-74339892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs185944925	chr12:74339919-74339920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111460084	chr12:74339920-74339921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546685596	chr12:74339969-74339970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528433047	chr12:74340035-74340036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148965496	chr12:74340036-74340037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Wilms tumour	21544195	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
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
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74326000-74326400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr12:74332400-74332600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:74339000-74339800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:74339400-74339800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:74339800-74343600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:74343400-74343600	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr12:74343400-74345000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr12:74343400-74345200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr12:74343600-74344600	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr12:74343600-74344800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:74343600-74344800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr12:74343600-74345200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:74343600-74346000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr12:74344000-74344600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr12:74344000-74344800	Enhancers	Brain Hippocampus Middle	brain
16	chr12:74344200-74344800	Enhancers	Brain Cingulate Gyrus	brain
17	chr12:74344200-74344800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr12:74344400-74344800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr12:74344600-74345000	Enhancers	Brain Anterior Caudate	brain
20	chr12:74344800-74345000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr12:74345000-74345800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:74345000-74346000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:74345200-74346000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr12:74345800-74346000	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
25	chr12:74345800-74346400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:74346000-74346200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr12:74346000-74346200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr12:74346400-74346600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr12:74367000-74368000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:74367200-74367600	Enhancers	Brain Germinal Matrix	brain
31	chr12:74367600-74368000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr12:74371800-74372200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr12:74390600-74391000	Enhancers	Brain Hippocampus Middle	brain
34	chr12:74404800-74405000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr12:74404800-74405600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr12:74404800-74406000	Enhancers	H1 Cell Line	embryonic stem cell
37	chr12:74404800-74406000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:74405400-74406200	Enhancers	Placenta Amnion	Placenta Amnion
39	chr12:74406200-74408200	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr12:74408200-74408400	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr12:74408200-74408600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr12:74408400-74408600	Enhancers	H9 Cell Line	embryonic stem cell
43	chr12:74408600-74413400	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr12:74411000-74411400	Enhancers	Liver	Liver
45	chr12:74411000-74411400	Enhancers	A549	lung
46	chr12:74411400-74415400	Weak transcription	A549	lung
47	chr12:74412000-74413000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr12:74412000-74413200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr12:74412200-74413000	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr12:74412400-74413000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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