Variant report

Variant	nsv966103
Chromosome Location	chr22:31410201-31452981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:525)
CpG islands
(count:0)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:525 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31440593-31440598	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:31451358-31452052	HepG2	liver:	n/a	n/a
3	ATF2	chr22:31451563-31451859	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr22:31451493-31452037	A549	lung:	n/a	n/a
5	ATF3	chr22:31444672-31444803	GM12878	blood:	n/a	n/a
6	ATF3	chr22:31451435-31451986	A549	lung:	n/a	n/a
7	ATF3	chr22:31451436-31451982	HepG2	liver:	n/a	n/a
8	ATF3	chr22:31444644-31444841	K562	blood:	n/a	n/a
9	ATF3	chr22:31451545-31451843	K562	blood:	n/a	n/a
10	ATF3	chr22:31451531-31452035	HCT-116	colon:	n/a	n/a
11	ATF3	chr22:31444606-31444820	GM12878	blood:	n/a	n/a
12	ATF3	chr22:31451550-31451912	HepG2	liver:	n/a	n/a
13	BCL3	chr22:31451375-31452047	A549	lung:	n/a	n/a
14	BCL3	chr22:31451404-31452226	A549	lung:	n/a	n/a
15	BHLHE40	chr22:31451552-31452058	HepG2	liver:	n/a	n/a
16	BRCA1	chr22:31451435-31451872	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr22:31413573-31413907	K562	blood:	n/a	n/a
18	CBX3	chr22:31425316-31425566	K562	blood:	n/a	n/a
19	CEBPB	chr22:31451503-31451967	IMR90	lung:	n/a	chr22:31451761-31451772
20	CEBPB	chr22:31451443-31452008	ECC-1	luminal epithelium:	n/a	chr22:31451761-31451772
21	CEBPB	chr22:31438755-31439029	K562	blood:	n/a	chr22:31438872-31438883
22	CEBPB	chr22:31432642-31432909	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr22:31451562-31451916	HepG2	liver:	n/a	chr22:31451761-31451772
24	CEBPB	chr22:31451549-31451997	HepG2	liver:	n/a	chr22:31451761-31451772
25	CEBPB	chr22:31451392-31452079	MCF-7	breast:	n/a	chr22:31451761-31451772
26	CEBPB	chr22:31418394-31418569	IMR90	lung:	n/a	n/a
27	CEBPB	chr22:31451343-31452150	A549	lung:	n/a	chr22:31451761-31451772
28	CEBPB	chr22:31451500-31451973	Hela-S3	cervix:	n/a	chr22:31451761-31451772
29	CEBPB	chr22:31442894-31443102	A549	lung:	n/a	chr22:31442931-31442942
30	CEBPB	chr22:31438768-31439018	HepG2	liver:	n/a	chr22:31438872-31438883
31	CEBPB	chr22:31451478-31451947	MCF-7	breast:	n/a	chr22:31451761-31451772
32	CEBPB	chr22:31438815-31439024	A549	lung:	n/a	chr22:31438872-31438883
33	CEBPB	chr22:31438814-31438981	IMR90	lung:	n/a	chr22:31438872-31438883
34	CEBPB	chr22:31451430-31451972	A549	lung:	n/a	chr22:31451761-31451772
35	CEBPB	chr22:31442913-31443015	Hela-S3	cervix:	n/a	chr22:31442931-31442942
36	CEBPB	chr22:31451539-31451970	ECC-1	luminal epithelium:	n/a	chr22:31451761-31451772
37	CEBPB	chr22:31418395-31418594	HepG2	liver:	n/a	n/a
38	CEBPB	chr22:31451506-31452012	HepG2	liver:	n/a	chr22:31451761-31451772
39	CEBPB	chr22:31451581-31451893	H1-hESC	embryonic stem cell:	n/a	chr22:31451761-31451772
40	CEBPB	chr22:31442793-31443097	HepG2	liver:	n/a	chr22:31442931-31442942
41	CEBPB	chr22:31451592-31451863	K562	blood:	n/a	chr22:31451761-31451772
42	CEBPB	chr22:31416483-31416601	HepG2	liver:	n/a	n/a
43	CEBPB	chr22:31442885-31443082	K562	blood:	n/a	chr22:31442931-31442942
44	CEBPB	chr22:31442795-31443112	IMR90	lung:	n/a	chr22:31442931-31442942
45	CEBPB	chr22:31451406-31451956	A549	lung:	n/a	chr22:31451761-31451772
46	CEBPB	chr22:31416432-31416701	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr22:31451491-31451995	HepG2	liver:	n/a	chr22:31451761-31451772
48	CEBPD	chr22:31451591-31451880	HepG2	liver:	n/a	n/a
49	CEBPD	chr22:31451549-31452004	HepG2	liver:	n/a	n/a
50	CHD2	chr22:31442784-31442836	H1-hESC	embryonic stem cell:	n/a	n/a

No data

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:31437736..31441147-chr22:31443914..31447179,4	K562	blood:
2	chr22:31439219..31443340-chr22:31479162..31482694,5	K562	blood:
3	chr22:31449984..31454484-chr22:31456787..31462654,7	K562	blood:
4	chr22:31431928..31434471-chr22:31449804..31451831,2	MCF-7	breast:
5	chr22:31421824..31424630-chr22:31434408..31437079,3	K562	blood:
6	chr22:31445325..31447022-chr22:31475452..31477796,2	MCF-7	breast:
7	chr22:31431282..31433620-chr22:31481041..31483644,2	MCF-7	breast:
8	chr22:31429286..31431329-chr22:31431481..31433428,2	MCF-7	breast:
9	chr22:31413340..31416231-chr22:31418212..31420315,2	K562	blood:
10	chr22:31432694..31433267-chr22:31544706..31545290,2	MCF-7	breast:
11	chr22:31430301..31432681-chr22:31434506..31436861,2	MCF-7	breast:
12	chr22:31363469..31366268-chr22:31450278..31456884,6	MCF-7	breast:
13	chr22:31432776..31435079-chr22:31450665..31453170,2	MCF-7	breast:
14	chr22:31416610..31418560-chr22:31480081..31482037,2	K562	blood:
15	chr22:31450684..31454190-chr22:31458624..31461519,3	K562	blood:
16	chr22:31452690..31454726-chr22:31460173..31463712,3	MCF-7	breast:
17	chr22:31440735..31445105-chr22:31479162..31482553,6	K562	blood:
18	chr22:31437736..31441147-chr22:31443914..31447179,4	K562	blood:
19	chr22:31445856..31448467-chr22:31451849..31454142,3	K562	blood:
20	chr22:31448944..31454267-chr22:31475725..31482456,15	MCF-7	breast:
21	chr22:31432776..31435079-chr22:31450665..31453170,2	MCF-7	breast:
22	chr22:31427554..31430340-chr22:31475829..31478342,2	MCF-7	breast:
23	chr22:31364474..31366749-chr22:31408252..31410827,2	MCF-7	breast:
24	chr22:31449294..31454779-chr22:31475265..31480255,11	MCF-7	breast:
25	chr22:31362787..31366384-chr22:31450123..31453347,3	MCF-7	breast:
26	chr22:31432480..31433175-chr22:31478482..31479318,2	MCF-7	breast:
27	chr22:31445377..31447360-chr22:31483123..31485957,2	MCF-7	breast:
28	chr22:31363146..31365916-chr22:31446912..31449134,2	MCF-7	breast:
29	chr22:31451720..31453462-chr22:31457824..31459739,2	MCF-7	breast:
30	chr22:31389318..31390927-chr22:31410868..31412701,2	MCF-7	breast:
31	chr22:31360377..31363179-chr22:31451258..31453241,3	K562	blood:
32	chr22:31450722..31454659-chr22:31476861..31481048,4	K562	blood:
33	chr22:31450083..31452668-chr22:31463620..31466392,3	MCF-7	breast:
34	chr22:31450718..31452880-chr22:31457371..31459942,3	MCF-7	breast:
35	chr22:31368025..31371169-chr22:31447828..31451638,3	MCF-7	breast:
36	chr22:31431928..31434471-chr22:31449804..31451831,2	MCF-7	breast:
37	chr22:31445856..31448467-chr22:31451849..31454142,3	K562	blood:
38	chr22:31430301..31432681-chr22:31434506..31436861,2	MCF-7	breast:
39	chr22:31413340..31416231-chr22:31418212..31420315,2	K562	blood:
40	chr22:31364027..31366021-chr22:31431032..31432822,2	MCF-7	breast:
41	chr13:30783910..30784430-chr22:31432453..31432955,2	MCF-7	breast:
42	chr22:31447674..31449826-chr22:31478695..31480363,2	K562	blood:
43	chr22:31421824..31424630-chr22:31434408..31437079,3	K562	blood:
44	chr22:31432694..31434751-chr22:31475361..31478726,3	MCF-7	breast:
45	chr22:31429286..31431329-chr22:31431481..31433428,2	MCF-7	breast:

No data

Variant related genes	Relation type
RN7SL633P	TF binding region
ENSG00000133422	chromatin interactions
ENSG00000273387	chromatin interactions
ENSG00000183963	chromatin interactions
ENSG00000253352	chromatin interactions

Extended variants
information (count: 1368 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1368 , 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	rs544003776	chr22:31410243-31410244	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576209184	chr22:31410261-31410262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564207224	chr22:31410268-31410269	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533020218	chr22:31410271-31410272	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540385299	chr22:31410329-31410330	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs5753425	chr22:31410356-31410357	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs563722615	chr22:31410363-31410364	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548983297	chr22:31410414-31410415	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372770168	chr22:31410435-31410436	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142134976	chr22:31410439-31410440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568943154	chr22:31410459-31410460	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151194432	chr22:31410474-31410475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531705806	chr22:31410514-31410515	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs141336119	chr22:31410540-31410541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146998866	chr22:31410576-31410577	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs180825041	chr22:31410589-31410590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs147645012	chr22:31410599-31410600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149561396	chr22:31410653-31410654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141512418	chr22:31410695-31410696	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553042738	chr22:31410711-31410712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567981573	chr22:31410712-31410713	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147029877	chr22:31410726-31410727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76230475	chr22:31410793-31410794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs185229671	chr22:31410798-31410799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs532356047	chr22:31410807-31410808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs117086032	chr22:31410843-31410844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372735086	chr22:31410844-31410845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557579992	chr22:31410845-31410846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189737764	chr22:31410897-31410898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558259307	chr22:31410906-31410907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572052357	chr22:31410926-31410927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540079364	chr22:31410967-31410968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375749557	chr22:31410985-31410986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138176677	chr22:31410987-31410988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529036088	chr22:31411021-31411022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542538698	chr22:31411047-31411048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562437705	chr22:31411066-31411067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546127750	chr22:31411088-31411089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149588613	chr22:31411110-31411111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565236833	chr22:31411139-31411140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527757327	chr22:31411144-31411145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143292517	chr22:31411211-31411212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183647101	chr22:31411215-31411216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572701808	chr22:31411216-31411217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372025086	chr22:31411226-31411227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148340943	chr22:31411242-31411243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550537473	chr22:31411265-31411266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189140424	chr22:31411273-31411274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570291078	chr22:31411306-31411307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545036131	chr22:31411335-31411336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
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	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20858604	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31409400-31413000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr22:31413000-31413400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr22:31413400-31415000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr22:31415000-31416000	Enhancers	Esophagus	oesophagus
5	chr22:31415000-31416600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr22:31415000-31416600	Enhancers	Placenta	Placenta
7	chr22:31415200-31417200	Enhancers	HepG2	liver
8	chr22:31415600-31415800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr22:31415600-31416600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr22:31416200-31417200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr22:31416400-31416600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr22:31416400-31416600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr22:31417600-31418800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr22:31417800-31418000	Enhancers	Rectal Smooth Muscle	rectum
15	chr22:31417800-31418600	Enhancers	Stomach Smooth Muscle	stomach
16	chr22:31418200-31418800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr22:31418400-31418800	Enhancers	Pancreas	Pancrea
18	chr22:31418400-31419600	Enhancers	Duodenum Mucosa	Duodenum
19	chr22:31419400-31419800	Enhancers	Stomach Mucosa	stomach
20	chr22:31429800-31430000	Enhancers	HepG2	liver
21	chr22:31430000-31434200	Weak transcription	HepG2	liver
22	chr22:31431000-31431800	Weak transcription	Stomach Smooth Muscle	stomach
23	chr22:31431400-31432600	Enhancers	Colon Smooth Muscle	Colon
24	chr22:31431600-31432400	Weak transcription	Fetal Intestine Small	intestine
25	chr22:31431600-31434600	Enhancers	Fetal Muscle Trunk	muscle
26	chr22:31431800-31432400	Enhancers	Stomach Smooth Muscle	stomach
27	chr22:31431800-31432600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr22:31431800-31432600	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr22:31431800-31432800	Enhancers	Fetal Muscle Leg	muscle
30	chr22:31431800-31432800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr22:31431800-31432800	Enhancers	NHEK	skin
32	chr22:31431800-31433000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr22:31431800-31433800	Enhancers	Duodenum Mucosa	Duodenum
34	chr22:31431800-31436000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr22:31431800-31437200	Enhancers	Fetal Stomach	stomach
36	chr22:31432000-31432400	Enhancers	Rectal Smooth Muscle	rectum
37	chr22:31432000-31433600	Enhancers	Placenta	Placenta
38	chr22:31432200-31432400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr22:31432200-31432600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr22:31432200-31432600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr22:31432200-31432800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr22:31432400-31432600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr22:31432400-31432600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr22:31432400-31432600	Enhancers	Muscle Satellite Cultured Cells	--
45	chr22:31432400-31432600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr22:31432400-31432600	Enhancers	Adipose Nuclei	Adipose
47	chr22:31432400-31432600	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr22:31432400-31432600	Enhancers	A549	lung
49	chr22:31432400-31432600	Enhancers	HSMMtube	muscle
50	chr22:31432400-31432600	Enhancers	NHDF-Ad	bronchial

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