Variant report

Variant	esv2762119
Chromosome Location	chr22:33006967-33101150
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1448)
CpG islands
(count:0)
Chromatin interactive
region (count:82)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1448 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:33076210-33076542	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:33046612-33046870	K562	blood:	n/a	n/a
3	ARID3A	chr22:33018519-33018704	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:33056291-33056543	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:33025168-33025484	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:33091315-33092167	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:33015113-33016307	HepG2	liver:	n/a	n/a
8	ARID3A	chr22:33045675-33045894	K562	blood:	n/a	n/a
9	ARID3A	chr22:33093358-33094099	HepG2	liver:	n/a	n/a
10	ARID3A	chr22:33040452-33040851	HepG2	liver:	n/a	n/a
11	ATF1	chr22:33072824-33073001	K562	blood:	n/a	n/a
12	ATF1	chr22:33080189-33080483	K562	blood:	n/a	n/a
13	ATF1	chr22:33045541-33045807	K562	blood:	n/a	n/a
14	ATF1	chr22:33081536-33081880	K562	blood:	n/a	n/a
15	ATF1	chr22:33089138-33089415	K562	blood:	n/a	n/a
16	ATF3	chr22:33045489-33045849	K562	blood:	n/a	n/a
17	BATF	chr22:33027126-33027419	GM12878	blood:	n/a	n/a
18	BCL3	chr22:33067260-33067596	GM12878	blood:	n/a	n/a
19	BCL3	chr22:33067286-33067942	GM12878	blood:	n/a	n/a
20	BHLHE40	chr22:33049994-33050139	K562	blood:	n/a	n/a
21	BHLHE40	chr22:33045553-33045754	K562	blood:	n/a	n/a
22	BHLHE40	chr22:33044936-33045036	K562	blood:	n/a	n/a
23	BHLHE40	chr22:33040230-33040919	HepG2	liver:	n/a	n/a
24	BHLHE40	chr22:33096388-33096755	K562	blood:	n/a	chr22:33096591-33096600 chr22:33096589-33096602 chr22:33096591-33096600 chr22:33096592-33096601 chr22:33096590-33096599 chr22:33096585-33096606
25	BHLHE40	chr22:33024318-33024333	HepG2	liver:	n/a	n/a
26	BHLHE40	chr22:33058036-33058366	K562	blood:	n/a	n/a
27	BHLHE40	chr22:33040414-33040726	HepG2	liver:	n/a	n/a
28	BHLHE40	chr22:33049737-33050137	HepG2	liver:	n/a	n/a
29	BHLHE40	chr22:33040369-33040718	K562	blood:	n/a	n/a
30	BHLHE40	chr22:33046671-33046677	K562	blood:	n/a	n/a
31	BHLHE40	chr22:33037049-33037234	K562	blood:	n/a	n/a
32	BRCA1	chr22:33040554-33040953	HepG2	liver:	n/a	n/a
33	BRCA1	chr22:33071144-33071677	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr22:33056267-33056531	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr22:33056343-33056450	GM12878	blood:	n/a	n/a
36	CBX3	chr22:33015922-33016147	K562	blood:	n/a	n/a
37	CEBPB	chr22:33097084-33097428	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr22:33056150-33056625	Hela-S3	cervix:	n/a	chr22:33056374-33056383
39	CEBPB	chr22:33093472-33093803	Hela-S3	cervix:	n/a	chr22:33093632-33093643
40	CEBPB	chr22:33056167-33056671	A549	lung:	n/a	chr22:33056374-33056383
41	CEBPB	chr22:33019910-33020087	K562	blood:	n/a	chr22:33020027-33020038
42	CEBPB	chr22:33056363-33056516	GM12878	blood:	n/a	chr22:33056374-33056383
43	CEBPB	chr22:33032975-33033341	MCF-7	breast:	n/a	n/a
44	CEBPB	chr22:33057295-33057752	IMR90	lung:	n/a	chr22:33057583-33057591 chr22:33057542-33057551 chr22:33057541-33057552
45	CEBPB	chr22:33089125-33089751	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr22:33056172-33056635	ECC-1	luminal epithelium:	n/a	chr22:33056374-33056383
47	CEBPB	chr22:33022031-33022304	K562	blood:	n/a	n/a
48	CEBPB	chr22:33025229-33025265	A549	lung:	n/a	chr22:33025248-33025259 chr22:33025247-33025260 chr22:33025247-33025258
49	CEBPB	chr22:33024986-33025594	HepG2	liver:	n/a	chr22:33025248-33025259 chr22:33025247-33025260 chr22:33025226-33025239 chr22:33025247-33025258
50	CEBPB	chr22:33056044-33056700	MCF-7	breast:	n/a	chr22:33056374-33056383

No data

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:33040520..33042023-chr22:33043962..33046745,2	MCF-7	breast:
2	22:32920308-32927723..22:33024278-33030812	Hela-S3	cervix:
3	chr22:33016718..33020351-chr22:33021844..33025503,4	K562	blood:
4	chr22:32924726..32925471-chr22:33055984..33056779,2	MCF-7	breast:
5	chr22:33048718..33051254-chr22:33053899..33056761,2	K562	blood:
6	chr22:32958043..32960588-chr22:33013928..33016358,2	MCF-7	breast:
7	chr22:33015941..33022634-chr22:33022783..33027992,6	MCF-7	breast:
8	chr22:32992332..32993916-chr22:33005017..33007101,2	MCF-7	breast:
9	chr22:33055970..33056871-chr22:33192363..33193467,3	K562	blood:
10	22:32145079-32150875..22:33084585-33087049	Hela-S3	cervix:
11	chr22:33040520..33042023-chr22:33043962..33046745,2	MCF-7	breast:
12	chr22:33056224..33058331-chr22:33096001..33097572,2	MCF-7	breast:
13	chr22:33061052..33063366-chr22:33066303..33069069,2	K562	blood:
14	chr22:33024320..33026626-chr22:33029132..33033030,5	MCF-7	breast:
15	chr22:33061052..33063366-chr22:33066303..33069069,2	K562	blood:
16	chr22:32955831..32960274-chr22:33021346..33026373,8	MCF-7	breast:
17	chr22:32953953..32955561-chr22:33025472..33027182,2	MCF-7	breast:
18	chr22:33016718..33020351-chr22:33021844..33025503,4	K562	blood:
19	chr22:33065425..33067736-chr22:33069316..33072006,2	MCF-7	breast:
20	22:32053085-32061138..22:33096044-33097202	Hela-S3	cervix:
21	chr22:33055973..33057208-chr22:33192214..33193923,10	MCF-7	breast:
22	chr22:33055951..33056920-chr22:33218725..33219416,2	MCF-7	breast:
23	chr22:33013961..33016702-chr22:33017273..33018854,2	MCF-7	breast:
24	chr22:33056224..33058331-chr22:33096001..33097572,2	MCF-7	breast:
25	chr22:33012442..33014400-chr22:33241656..33243487,2	K562	blood:
26	chr22:32955723..32958246-chr22:33022989..33024633,3	MCF-7	breast:
27	chr22:33067760..33069743-chr22:33076453..33078669,2	MCF-7	breast:
28	chr22:33067760..33069743-chr22:33076453..33078669,2	MCF-7	breast:
29	22:32920308-32927723..22:33097202-33103208	Hela-S3	cervix:
30	22:32477762-32487457..22:33097202-33103208	GM12878	blood:
31	22:33084585-33087049..22:33262063-33266567	Hela-S3	cervix:
32	chr22:32969893..32972512-chr22:33046194..33048392,2	MCF-7	breast:
33	22:32920308-32927723..22:33052831-33056804	K562	blood:
34	22:32920308-32927723..22:33084585-33087049	Hela-S3	cervix:
35	22:32915608-32918105..22:33084585-33087049	K562	blood:
36	chr22:33014781..33017660-chr22:33019637..33021375,2	MCF-7	breast:
37	22:32264718-32278135..22:33097202-33103208	GM12878	blood:
38	chr22:33021627..33024969-chr22:33195694..33198618,3	MCF-7	breast:
39	chr22:32924655..32925584-chr22:33042020..33042779,2	K562	blood:
40	chr22:33065425..33067736-chr22:33069316..33072006,2	MCF-7	breast:
41	chr22:33054648..33057436-chr22:33186906..33189165,2	MCF-7	breast:
42	22:32920308-32927723..22:33096044-33097202	Hela-S3	cervix:
43	chr22:33056115..33056811-chr22:33192659..33193956,7	MCF-7	breast:
44	chr22:32957485..32959832-chr22:33020527..33022697,2	MCF-7	breast:
45	chr22:33086623..33088855-chr22:33091258..33093872,2	MCF-7	breast:
46	chr22:33013961..33016702-chr22:33017273..33018854,2	MCF-7	breast:
47	22:32920308-32927723..22:33022020-33023623	H1-hESC	embryonic stem cell:	embryo
48	chr22:33054576..33056932-chr22:33196942..33199006,3	MCF-7	breast:
49	22:33002359-33009462..22:33262063-33266567	Hela-S3	cervix:
50	chr22:32870581..32872197-chr22:33054126..33056374,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-2	chr22:33048403-33048415	ENSG00000251658

No data

Variant related genes	Relation type
RNA5SP497	TF binding region
ENSG00000205853	chromatin interactions
ENSG00000271093	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000183530	chromatin interactions
ENSG00000251890	chromatin interactions
ENSG00000100225	chromatin interactions
ENSG00000100234	chromatin interactions
ENSG00000100170	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000185666	chromatin interactions
ENSG00000100150	chromatin interactions
ENSG00000128276	chromatin interactions
IP6K1	miRNA target sites

Extended variants
information (count: 2744 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2744 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5994593	chr22:33006967-33006968	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74922324	chr22:33007015-33007016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs545692364	chr22:33007023-33007024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs386820761	chr22:33007038-33007039	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184141301	chr22:33007040-33007041	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552939343	chr22:33007042-33007043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs561648052	chr22:33007051-33007052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536538536	chr22:33007052-33007053	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149457345	chr22:33007059-33007060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs143973673	chr22:33007075-33007076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs60966625	chr22:33007142-33007143	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573326510	chr22:33007163-33007164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148633475	chr22:33007164-33007165	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536046521	chr22:33007198-33007199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545426926	chr22:33007204-33007205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369814600	chr22:33007222-33007223	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190710582	chr22:33007227-33007228	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569548589	chr22:33007264-33007265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544698895	chr22:33007270-33007271	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs2710392	chr22:33007271-33007272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200168140	chr22:33007277-33007278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs11705031	chr22:33007293-33007294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs181839980	chr22:33007311-33007312	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142179727	chr22:33007312-33007313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558096116	chr22:33007323-33007324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs578048499	chr22:33007331-33007332	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2710393	chr22:33007343-33007344	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs553966514	chr22:33007362-33007363	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs5749472	chr22:33007374-33007375	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs541602877	chr22:33007379-33007380	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113289569	chr22:33007404-33007405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs186373111	chr22:33007415-33007416	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189199866	chr22:33007443-33007444	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543887106	chr22:33007482-33007483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111782519	chr22:33007494-33007495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532894191	chr22:33007507-33007508	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181555401	chr22:33007513-33007514	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61110043	chr22:33007514-33007515	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs2858744	chr22:33007543-33007544	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549580401	chr22:33007547-33007548	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140559384	chr22:33007651-33007652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs112495342	chr22:33007655-33007656	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs75019831	chr22:33007706-33007707	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551496622	chr22:33007729-33007730	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571656811	chr22:33007756-33007757	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs202121393	chr22:33007827-33007828	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs375245944	chr22:33007882-33007883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554272367	chr22:33007890-33007891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368252463	chr22:33008007-33008008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573781392	chr22:33008012-33008013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
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
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
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33002600-33009800	Weak transcription	Fetal Kidney	kidney
2	chr22:33004000-33008800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr22:33004000-33009400	Weak transcription	Spleen	Spleen
4	chr22:33004000-33011600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr22:33004000-33011600	Weak transcription	Placenta	Placenta
6	chr22:33004000-33011800	Weak transcription	Left Ventricle	heart
7	chr22:33004000-33012600	Weak transcription	Fetal Lung	lung
8	chr22:33008800-33010600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr22:33009400-33010200	Enhancers	Spleen	Spleen
10	chr22:33009800-33010200	Enhancers	Fetal Heart	heart
11	chr22:33009800-33010400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr22:33009800-33010400	Enhancers	Fetal Kidney	kidney
13	chr22:33009800-33010400	Enhancers	Lung	lung
14	chr22:33009800-33010600	Enhancers	Fetal Stomach	stomach
15	chr22:33010200-33010400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:33010200-33010400	Enhancers	Fetal Muscle Leg	muscle
17	chr22:33010200-33010600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr22:33010200-33011800	Weak transcription	Fetal Heart	heart
19	chr22:33010200-33012400	Weak transcription	Spleen	Spleen
20	chr22:33010400-33010600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr22:33010400-33010600	Enhancers	Right Ventricle	heart
22	chr22:33010400-33011600	Weak transcription	Fetal Muscle Leg	muscle
23	chr22:33010400-33011800	Weak transcription	Lung	lung
24	chr22:33010400-33013000	Weak transcription	Fetal Kidney	kidney
25	chr22:33010400-33017400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr22:33010600-33011400	Weak transcription	Fetal Stomach	stomach
27	chr22:33010600-33011600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr22:33010600-33011800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr22:33010600-33012000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr22:33010600-33012000	Weak transcription	Right Ventricle	heart
31	chr22:33011400-33011800	Enhancers	HepG2	liver
32	chr22:33011400-33015800	Enhancers	Fetal Stomach	stomach
33	chr22:33011600-33012200	Enhancers	H1 Cell Line	embryonic stem cell
34	chr22:33011600-33012200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr22:33011600-33012400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr22:33011600-33012600	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr22:33011600-33012600	Enhancers	Placenta	Placenta
38	chr22:33011600-33015000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr22:33011600-33015200	Enhancers	Fetal Muscle Trunk	muscle
40	chr22:33011600-33015200	Enhancers	Fetal Muscle Leg	muscle
41	chr22:33011800-33012000	Enhancers	Psoas Muscle	Psoas
42	chr22:33011800-33012000	Enhancers	Rectal Smooth Muscle	rectum
43	chr22:33011800-33012200	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr22:33011800-33012200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr22:33011800-33012400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr22:33011800-33012600	Enhancers	Fetal Heart	heart
47	chr22:33011800-33012600	Enhancers	Lung	lung
48	chr22:33011800-33012600	Enhancers	Right Atrium	heart
49	chr22:33011800-33012800	Flanking Active TSS	HepG2	liver
50	chr22:33011800-33013000	Enhancers	Left Ventricle	heart

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