Variant report

Variant	nsv459864
Chromosome Location	chr22:27760086-27865344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1138)
CpG islands
(count:427)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1138 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:27769488-27769544	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:27858256-27858552	HepG2	liver:	n/a	n/a
3	BACH1	chr22:27851013-27851014	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr22:27779416-27779513	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr22:27779248-27779526	K562	blood:	n/a	n/a
6	BACH1	chr22:27849743-27849959	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr22:27812863-27812889	K562	blood:	n/a	n/a
8	BHLHE40	chr22:27800536-27800675	K562	blood:	n/a	chr22:27800597-27800606 chr22:27800598-27800607 chr22:27800595-27800608 chr22:27800597-27800606 chr22:27800596-27800605 chr22:27800591-27800612
9	BHLHE40	chr22:27766250-27766608	K562	blood:	n/a	n/a
10	BHLHE40	chr22:27783696-27783896	HepG2	liver:	n/a	n/a
11	BHLHE40	chr22:27811840-27812026	K562	blood:	n/a	n/a
12	BRCA1	chr22:27801966-27802162	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr22:27858110-27858278	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr22:27827809-27828304	HCT-116	colon:	n/a	n/a
15	CEBPB	chr22:27801960-27802126	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr22:27807373-27807484	A549	lung:	n/a	n/a
17	CEBPB	chr22:27859025-27859065	HepG2	liver:	n/a	n/a
18	CEBPB	chr22:27830901-27831271	HepG2	liver:	n/a	chr22:27831045-27831058
19	CEBPB	chr22:27830914-27831198	A549	lung:	n/a	chr22:27831045-27831058
20	CEBPB	chr22:27830948-27831171	K562	blood:	n/a	chr22:27831045-27831058
21	CEBPB	chr22:27794072-27794253	HepG2	liver:	n/a	n/a
22	CEBPB	chr22:27807358-27807495	IMR90	lung:	n/a	n/a
23	CEBPB	chr22:27830957-27831202	IMR90	lung:	n/a	chr22:27831045-27831058
24	CEBPB	chr22:27858249-27858545	HepG2	liver:	n/a	n/a
25	CEBPB	chr22:27792980-27793272	A549	lung:	n/a	chr22:27793243-27793255
26	CEBPB	chr22:27816596-27816951	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr22:27830987-27831224	H1-hESC	embryonic stem cell:	n/a	chr22:27831045-27831058
28	CEBPB	chr22:27793904-27794357	IMR90	lung:	n/a	n/a
29	CEBPB	chr22:27793102-27793287	IMR90	lung:	n/a	chr22:27793243-27793255
30	CEBPB	chr22:27807376-27807556	HepG2	liver:	n/a	n/a
31	CEBPB	chr22:27830885-27831288	A549	lung:	n/a	chr22:27831045-27831058
32	CEBPB	chr22:27794166-27794272	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr22:27792741-27793059	HepG2	liver:	n/a	n/a
34	CEBPB	chr22:27812986-27813230	IMR90	lung:	n/a	n/a
35	CHD2	chr22:27801883-27802083	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr22:27769188-27769212	K562	blood:	n/a	n/a
37	CHD2	chr22:27769370-27769555	HepG2	liver:	n/a	n/a
38	CHD2	chr22:27813127-27813409	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr22:27766308-27766526	K562	blood:	n/a	n/a
40	CHD2	chr22:27766342-27766498	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr22:27769244-27769574	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr22:27801868-27802143	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr22:27829717-27829847	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTBP2	chr22:27857413-27857767	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTBP2	chr22:27812550-27813463	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr22:27778100-27778250	BE2_C	brain:	n/a	n/a
47	CTCF	chr22:27805320-27805470	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr22:27778012-27778262	HepG2	liver:	n/a	n/a
49	CTCF	chr22:27794060-27794210	HPF	lung:	n/a	n/a
50	CTCF	chr22:27801912-27802167	Pancreas_OC	pancreas:	n/a	chr22:27802043-27802064 chr22:27802041-27802059 chr22:27802042-27802058

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:27834439-27834489	RPTEC	kidney:	n/a
2	chr22:27838621-27838671	A549	lung:	n/a
3	chr22:27831818-27831868	AoSMC	blood vessel:	n/a
4	chr22:27834439-27834489	NHBE	bronchial:	n/a
5	chr22:27835596-27835646	Jurkat	blood:	n/a
6	chr22:27834439-27834489	GM19239	blood:	n/a
7	chr22:27834549-27834599	HMEC	breast:	n/a
8	chr22:27838621-27838671	HCPEpiC	choroid plexus:	n/a
9	chr22:27831818-27831868	HEEpiC	esophagus:	n/a
10	chr22:27831818-27831868	AG09309	skin:	n/a
11	chr22:27832684-27832734	GM19239	blood:	n/a
12	chr22:27838621-27838671	SK-N-MC	brain:	n/a
13	chr22:27834629-27834679	HCT-116	colon:	n/a
14	chr22:27835596-27835646	HEK293	kidney:	embryo
15	chr22:27834439-27834489	CMK	blood:	n/a
16	chr22:27834439-27834489	HRE	kidney:	n/a
17	chr22:27834439-27834489	NHDF-neo	bronchial:	n/a
18	chr22:27834549-27834599	AoSMC	blood vessel:	n/a
19	chr22:27835596-27835646	NHDF-neo	bronchial:	n/a
20	chr22:27834439-27834489	HNPCEpiC	eye:	n/a
21	chr22:27832684-27832734	U87	brain:	n/a
22	chr22:27834629-27834679	MCF10A-Er-Src	breast:	n/a
23	chr22:27834629-27834679	NT2-D1	testis:	n/a
24	chr22:27832684-27832734	HL-60	blood:	n/a
25	chr22:27834629-27834679	SAEC	small airway:	n/a
26	chr22:27832684-27832734	HAEpiC	amniotic membrane:	n/a
27	chr22:27835596-27835646	SAEC	small airway:	n/a
28	chr22:27831818-27831868	ovcar-3	ovarian:	n/a
29	chr22:27835596-27835646	NH-A	brain:	n/a
30	chr22:27834549-27834599	HRPEpiC	eye:	n/a
31	chr22:27832684-27832734	NHBE	bronchial:	n/a
32	chr22:27834629-27834679	A549	lung:	n/a
33	chr22:27838621-27838671	HMEC	breast:	n/a
34	chr22:27835596-27835646	PFSK-1	brain:	n/a
35	chr22:27834439-27834489	AoSMC	blood vessel:	n/a
36	chr22:27834549-27834599	HNPCEpiC	eye:	n/a
37	chr22:27835596-27835646	AG04449	skin:	fetal
38	chr22:27834549-27834599	SKMC	muscle:	n/a
39	chr22:27834549-27834599	HEK293	kidney:	embryo
40	chr22:27834439-27834489	Caco-2	colon:	n/a
41	chr22:27831818-27831868	AG10803	skin:	n/a
42	chr22:27834439-27834489	HCT-116	colon:	n/a
43	chr22:27832684-27832734	SKMC	muscle:	n/a
44	chr22:27838621-27838671	U87	brain:	n/a
45	chr22:27832684-27832734	MCF-7	breast:	n/a
46	chr22:27835596-27835646	SK-N-SH_RA	brain:	n/a
47	chr22:27834439-27834489	SK-N-SH	brain:	n/a
48	chr22:27835596-27835646	HCT-116	colon:	n/a
49	chr22:27832684-27832734	HCT-116	colon:	n/a
50	chr22:27832684-27832734	AG04449	skin:	fetal

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:27758823..27761385-chr22:27766843..27769713,2	K562	blood:
2	chr22:27801836..27802493-chr22:27883347..27884309,2	MCF-7	breast:
3	chr22:27824367..27826325-chr22:27829603..27833358,3	K562	blood:
4	chr22:27777645..27778297-chr22:27830082..27831081,2	MCF-7	breast:
5	chr22:27801584..27802512-chr22:28200419..28200949,3	MCF-7	breast:
6	chr22:27765218..27767884-chr22:27773651..27775171,2	MCF-7	breast:
7	chr22:27828309..27830905-chr22:27832011..27834515,2	K562	blood:
8	chr22:27780012..27781699-chr22:27782011..27784534,2	MCF-7	breast:
9	chr22:27777645..27778297-chr22:27830082..27831081,2	MCF-7	breast:
10	chr22:27824367..27826325-chr22:27829603..27833358,3	K562	blood:
11	chr22:27801848..27804523-chr22:27818644..27820694,2	MCF-7	breast:
12	chr22:27741067..27741629-chr22:27773951..27774489,2	MCF-7	breast:
13	chr22:27828309..27830905-chr22:27832011..27834515,2	K562	blood:
14	chr22:27857934..27860311-chr22:27860712..27862590,2	K562	blood:
15	chr22:27765218..27767884-chr22:27773651..27775171,2	MCF-7	breast:
16	chr22:27813673..27816169-chr22:27820833..27822951,2	MCF-7	breast:
17	chr22:27803590..27805944-chr22:27807560..27809158,2	MCF-7	breast:
18	chr22:27801863..27802520-chr22:28276059..28277086,3	MCF-7	breast:
19	chr22:27801848..27804523-chr22:27818644..27820694,2	MCF-7	breast:
20	chr22:27803590..27805944-chr22:27807560..27809158,2	MCF-7	breast:
21	chr22:27780012..27781699-chr22:27782011..27784534,2	MCF-7	breast:
22	chr22:27823489..27825867-chr22:27829603..27831710,2	K562	blood:
23	chr22:27832758..27834628-chr22:27836553..27838416,2	MCF-7	breast:
24	chr22:27758823..27761385-chr22:27766843..27769713,2	K562	blood:
25	chr22:27813673..27816169-chr22:27820833..27822951,2	MCF-7	breast:
26	chr22:27857934..27860311-chr22:27860712..27862590,2	K562	blood:
27	chr22:27753926..27755541-chr22:27761401..27764345,2	MCF-7	breast:
28	chr22:27823489..27825867-chr22:27829603..27831710,2	K562	blood:
29	chr22:27068183..27070015-chr22:27791994..27793876,2	MCF-7	breast:
30	chr22:27832758..27834628-chr22:27836553..27838416,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MN1-4	chr22:27855736-27856021	XLOC_014330
2	lnc-CRYBA4-9	chr22:27775147-27775226	XLOC_014198
3	lnc-MN1-4	chr22:27853208-27853691	XLOC_014330

No data

Variant related genes	Relation type
ENSG00000227880	TF binding region
ENSG00000227880	CpG island
ENSG00000244625	chromatin interactions
ENSG00000206028	chromatin interactions
VCL	miRNA target sites
PHF12	miRNA target sites

Extended variants
information (count: 4547 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4547 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76804280	chr22:27761425-27761426	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs529120798	chr22:27761441-27761442	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs144587226	chr22:27761459-27761460	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs531496782	chr22:27761466-27761467	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs550022482	chr22:27761491-27761492	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs12168409	chr22:27761508-27761509	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs557997790	chr22:27764823-27764824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556706173	chr22:27764851-27764852	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566795357	chr22:27764854-27764855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377252427	chr22:27764941-27764942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369795297	chr22:27764961-27764962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189138006	chr22:27764983-27764984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553438644	chr22:27764994-27764995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574979197	chr22:27765014-27765015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542357591	chr22:27765021-27765022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567296549	chr22:27765023-27765024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557180283	chr22:27765042-27765043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs5997238	chr22:27765064-27765065	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs546099636	chr22:27765075-27765076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140231440	chr22:27765088-27765089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117357062	chr22:27765105-27765106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539831405	chr22:27765194-27765195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561392183	chr22:27765199-27765200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575881568	chr22:27765220-27765221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201760099	chr22:27765221-27765222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181506093	chr22:27765254-27765255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187661393	chr22:27765257-27765258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573071983	chr22:27765270-27765271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568874005	chr22:27765271-27765272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533122208	chr22:27765299-27765300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191932631	chr22:27765321-27765322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544875828	chr22:27765325-27765326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566758722	chr22:27765327-27765328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181027528	chr22:27765329-27765330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376426453	chr22:27765366-27765367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553401783	chr22:27765367-27765368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145915871	chr22:27765372-27765373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148162645	chr22:27765378-27765379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141961221	chr22:27765415-27765416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546343404	chr22:27765417-27765418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575674209	chr22:27765418-27765419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546361142	chr22:27765427-27765428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150659510	chr22:27765433-27765434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138819419	chr22:27765438-27765439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540477002	chr22:27765442-27765443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562053472	chr22:27765448-27765449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573266014	chr22:27765468-27765469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543770267	chr22:27765473-27765474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184992598	chr22:27765491-27765492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532920887	chr22:27765504-27765505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Cancer	21183584	CNVD
Breast cancer	17142309	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:1428 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27761400-27761600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr22:27764800-27765000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr22:27765000-27765200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr22:27765000-27765200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr22:27765000-27765200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr22:27765000-27765400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr22:27765200-27766000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr22:27765200-27766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr22:27765200-27768800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr22:27765400-27765800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr22:27765600-27765800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr22:27765600-27765800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr22:27765600-27766600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr22:27765800-27766400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr22:27765800-27767000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr22:27765800-27769000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr22:27766000-27766200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr22:27766000-27766200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr22:27766000-27766400	Enhancers	Primary hematopoietic stem cells	blood
20	chr22:27766000-27766400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr22:27766000-27766600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr22:27766200-27766600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr22:27766200-27768600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr22:27766200-27769000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr22:27766400-27766600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr22:27766400-27769000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr22:27766400-27769000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr22:27766600-27768800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr22:27766600-27769000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr22:27766600-27769000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr22:27767000-27767400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr22:27767200-27767400	Enhancers	Pancreas	Pancrea
33	chr22:27767400-27768400	Weak transcription	Pancreas	Pancrea
34	chr22:27767400-27769600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr22:27768200-27768400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr22:27768400-27768600	Enhancers	Pancreas	Pancrea
37	chr22:27768400-27769800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr22:27768600-27768800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr22:27768600-27769000	Weak transcription	Pancreas	Pancrea
40	chr22:27768800-27769000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr22:27768800-27769000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr22:27768800-27769000	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr22:27768800-27769000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr22:27768800-27769000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr22:27768800-27769000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
46	chr22:27768800-27769200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr22:27768800-27769400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr22:27769000-27769200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
49	chr22:27769000-27769200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr22:27769000-27769400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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