Variant report

Variant	nsv3589
Chromosome Location	chr22:29265164-29288935
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29283090-29284174	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:29281876-29282369	HepG2	liver:	n/a	n/a
3	ATF3	chr22:29269502-29270005	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr22:29279473-29279689	HepG2	liver:	n/a	chr22:29279551-29279560
5	ATF3	chr22:29269587-29269914	K562	blood:	n/a	n/a
6	ATF3	chr22:29269529-29269922	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr22:29279478-29279629	K562	blood:	n/a	chr22:29279551-29279560
8	BACH1	chr22:29279963-29280004	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr22:29279533-29279602	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr22:29279396-29280060	K562	blood:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29279641-29279657
11	BHLHE40	chr22:29275871-29276245	GM12878	blood:	n/a	n/a
12	BHLHE40	chr22:29278447-29279161	K562	blood:	n/a	chr22:29278642-29278651 chr22:29278641-29278650 chr22:29278641-29278650
13	BHLHE40	chr22:29279330-29279751	HepG2	liver:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29279641-29279657
14	BHLHE40	chr22:29278529-29278853	GM12878	blood:	n/a	chr22:29278642-29278651 chr22:29278641-29278650 chr22:29278641-29278650
15	BHLHE40	chr22:29278522-29279769	HepG2	liver:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29278642-29278651 chr22:29278641-29278650 chr22:29279641-29279657 chr22:29278641-29278650
16	BHLHE40	chr22:29279400-29279762	GM12878	blood:	n/a	chr22:29279640-29279656 chr22:29279457-29279473 chr22:29279643-29279659 chr22:29279490-29279506 chr22:29279641-29279657
17	BHLHE40	chr22:29280016-29280063	GM12878	blood:	n/a	n/a
18	BHLHE40	chr22:29281163-29281177	K562	blood:	n/a	n/a
19	BHLHE40	chr22:29278584-29278808	A549	lung:	n/a	chr22:29278642-29278651 chr22:29278641-29278650 chr22:29278641-29278650
20	BHLHE40	chr22:29279424-29279627	HepG2	liver:	n/a	chr22:29279457-29279473 chr22:29279490-29279506
21	BRCA1	chr22:29279494-29279583	Hela-S3	cervix:	n/a	n/a
22	CCNT2	chr22:29278612-29279774	K562	blood:	n/a	chr22:29279418-29279427 chr22:29279408-29279417
23	CEBPB	chr22:29276795-29276980	HepG2	liver:	n/a	chr22:29276910-29276921
24	CEBPB	chr22:29276793-29276978	K562	blood:	n/a	chr22:29276910-29276921
25	CEBPB	chr22:29274192-29274349	K562	blood:	n/a	n/a
26	CEBPB	chr22:29279868-29280076	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr22:29279897-29280088	IMR90	lung:	n/a	n/a
28	CEBPB	chr22:29276779-29277083	IMR90	lung:	n/a	chr22:29276910-29276921
29	CEBPB	chr22:29279071-29279430	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr22:29282019-29282048	A549	lung:	n/a	n/a
31	CEBPB	chr22:29279946-29280025	K562	blood:	n/a	n/a
32	CEBPD	chr22:29278894-29279304	HepG2	liver:	n/a	n/a
33	CEBPD	chr22:29279365-29279771	HepG2	liver:	n/a	n/a
34	CHD1	chr22:29279972-29280045	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr22:29280047-29280061	HepG2	liver:	n/a	n/a
36	CHD2	chr22:29278823-29279261	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr22:29278891-29279098	K562	blood:	n/a	n/a
38	CHD2	chr22:29279516-29279591	HepG2	liver:	n/a	n/a
39	CHD2	chr22:29278821-29279143	HepG2	liver:	n/a	n/a
40	CHD2	chr22:29279898-29280058	K562	blood:	n/a	n/a
41	CHD2	chr22:29279476-29279634	H1-hESC	embryonic stem cell:	n/a	chr22:29279606-29279616
42	CHD2	chr22:29279599-29279636	K562	blood:	n/a	chr22:29279606-29279616
43	CHD2	chr22:29280527-29280553	HepG2	liver:	n/a	n/a
44	CHD2	chr22:29279944-29280126	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr22:29278933-29279658	Hela-S3	cervix:	n/a	chr22:29279606-29279616 chr22:29279409-29279419
46	CHD2	chr22:29280737-29280925	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr22:29280358-29280359	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr22:29278931-29279515	GM12878	blood:	n/a	chr22:29279409-29279419
49	CREB1	chr22:29279009-29279748	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr22:29278932-29279755	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29279967-29280017	HIPEpiC	eye:	n/a
2	chr22:29284199-29284249	HMEC	breast:	n/a
3	chr22:29281173-29281223	GM12878	blood:	n/a
4	chr22:29279592-29279642	HPAEpiC	pulmonary alveolar:	n/a
5	chr22:29279592-29279642	AG10803	skin:	n/a
6	chr22:29284199-29284249	HCT-116	colon:	n/a
7	chr22:29281173-29281223	RPTEC	kidney:	n/a
8	chr22:29279592-29279642	GM12878	blood:	n/a
9	chr22:29279129-29279179	U87	brain:	n/a
10	chr22:29284199-29284249	U87	brain:	n/a
11	chr22:29280932-29280982	Jurkat	blood:	n/a
12	chr22:29279129-29279179	HRCEpiC	kidney:	n/a
13	chr22:29279203-29279253	ovcar-3	ovarian:	n/a
14	chr22:29278230-29278280	NB4	blood:	n/a
15	chr22:29284199-29284249	NHDF-neo	bronchial:	n/a
16	chr22:29284199-29284249	RPTEC	kidney:	n/a
17	chr22:29279129-29279179	HCT-116	colon:	n/a
18	chr22:29280932-29280982	HCPEpiC	choroid plexus:	n/a
19	chr22:29280932-29280982	HCT-116	colon:	n/a
20	chr22:29279203-29279253	AoSMC	blood vessel:	n/a
21	chr22:29278230-29278280	PANC-1	pancreas:	n/a
22	chr22:29279967-29280017	NT2-D1	testis:	n/a
23	chr22:29278230-29278280	SK-N-SH	brain:	n/a
24	chr22:29279592-29279642	SAEC	small airway:	n/a
25	chr22:29279597-29279647	NHBE	bronchial:	n/a
26	chr22:29279597-29279647	GM06990	blood:	n/a
27	chr22:29280932-29280982	Hela-S3	cervix:	n/a
28	chr22:29280932-29280982	HRPEpiC	eye:	n/a
29	chr22:29279597-29279647	HEK293	kidney:	embryo
30	chr22:29279129-29279179	HAEpiC	amniotic membrane:	n/a
31	chr22:29281173-29281223	HRCEpiC	kidney:	n/a
32	chr22:29275887-29275937	NB4	blood:	n/a
33	chr22:29279967-29280017	NHBE	bronchial:	n/a
34	chr22:29280180-29280230	AG09319	gingival:	n/a
35	chr22:29279129-29279179	HCM	heart:	n/a
36	chr22:29279592-29279642	HRE	kidney:	n/a
37	chr22:29279592-29279642	NB4	blood:	n/a
38	chr22:29279129-29279179	NB4	blood:	n/a
39	chr22:29280932-29280982	BE2_C	brain:	n/a
40	chr22:29278230-29278280	LNCaP	prostate:	n/a
41	chr22:29279597-29279647	PrEC	prostate:	n/a
42	chr22:29279129-29279179	Jurkat	blood:	n/a
43	chr22:29280180-29280230	T-47D	breast:	n/a
44	chr22:29280932-29280982	LNCaP	prostate:	n/a
45	chr22:29279597-29279647	BJ	skin:	n/a
46	chr22:29279967-29280017	ECC-1	luminal epithelium:	n/a
47	chr22:29279129-29279179	HCF	heart:	n/a
48	chr22:29275887-29275937	AG04450	lung:	fetal
49	chr22:29279129-29279179	MCF10A-Er-Src	breast:	n/a
50	chr22:29281173-29281223	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:29274825..29277296-chr22:29277384..29279241,2	K562	blood:
2	chr22:29269063..29271237-chr22:29276306..29278177,2	MCF-7	breast:
3	chr22:29280624..29284164-chr22:29307760..29311501,3	MCF-7	breast:
4	chr22:29273841..29275585-chr22:29663664..29665698,2	K562	blood:
5	chr16:31128850..31129465-chr22:29279200..29279987,2	Hela-S3	cervix:
6	chr22:29279568..29281765-chr22:29467462..29470387,2	K562	blood:
7	chr22:29283926..29288290-chr22:29291343..29295207,5	K562	blood:
8	chr22:29270216..29271943-chr22:29278267..29281046,2	K562	blood:
9	chr22:29274825..29277296-chr22:29277384..29279241,2	K562	blood:
10	chr22:29269063..29271237-chr22:29276306..29278177,2	MCF-7	breast:
11	chr22:29269180..29273924-chr22:29276506..29281046,6	K562	blood:
12	chr22:29210544..29212146-chr22:29276530..29279392,2	MCF-7	breast:
13	chr22:29277854..29280834-chr3:15899899..15902425,2	MCF-7	breast:
14	chr22:29195360..29197093-chr22:29263456..29265495,2	K562	blood:
15	chr22:29279139..29280999-chr22:29287403..29288921,2	K562	blood:
16	chr22:29275445..29276268-chr22:29488136..29488887,2	MCF-7	breast:
17	chr22:29277392..29281683-chr22:29281887..29284497,5	MCF-7	breast:
18	chr22:29287874..29289699-chr22:29289743..29291246,2	K562	blood:
19	chr22:29275977..29281461-chr22:29425203..29430435,9	MCF-7	breast:
20	chr22:29280662..29283145-chr22:29436035..29437760,2	K562	blood:
21	chr22:29262040..29263818-chr22:29273723..29275867,2	K562	blood:
22	chr22:29194507..29196726-chr22:29278986..29282462,3	MCF-7	breast:
23	chr22:29278420..29281129-chr22:29285869..29288774,2	K562	blood:
24	chr22:29137399..29139735-chr22:29278518..29281229,2	MCF-7	breast:
25	chr22:29280249..29282213-chr22:29433685..29436671,2	MCF-7	breast:
26	chr22:29278902..29281359-chr22:29283717..29285829,4	K562	blood:

Variant related genes	Relation type
ZNRF3	TF binding region
ZNRF3	CpG island
ENSG00000183579	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000177993	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000272858	chromatin interactions
ENSG00000262766	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000103510	chromatin interactions
ENSG00000183762	chromatin interactions
ENSG00000206560	chromatin interactions
ENSG00000183765	chromatin interactions

Extended variants
information (count: 805 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544610350	chr22:29265194-29265195	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140245618	chr22:29265211-29265212	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs145203476	chr22:29265212-29265213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs12166788	chr22:29265222-29265223	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs555584106	chr22:29265255-29265256	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs148168929	chr22:29265311-29265312	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs187021812	chr22:29265316-29265317	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12170985	chr22:29265336-29265337	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371207037	chr22:29265372-29265373	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536548950	chr22:29265483-29265484	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs141973190	chr22:29265508-29265509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs5762873	chr22:29265512-29265513	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569108338	chr22:29265575-29265576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551814341	chr22:29265606-29265607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368835542	chr22:29265609-29265610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138699787	chr22:29265610-29265611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566890655	chr22:29265655-29265656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs59264876	chr22:29265681-29265682	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs367809619	chr22:29265695-29265696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74987813	chr22:29265776-29265777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537662406	chr22:29265892-29265893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555995680	chr22:29265902-29265903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577540345	chr22:29265927-29265928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374043769	chr22:29265938-29265939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150258034	chr22:29265972-29265973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs5752822	chr22:29266025-29266026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs535906522	chr22:29266049-29266050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555566318	chr22:29266058-29266059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs62235752	chr22:29266094-29266095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76852457	chr22:29266095-29266096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542355871	chr22:29266138-29266139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561079847	chr22:29266140-29266141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73388855	chr22:29266144-29266145	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs548155749	chr22:29266146-29266147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369805663	chr22:29266188-29266189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563140284	chr22:29266297-29266298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs67512854	chr22:29266310-29266311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541642569	chr22:29266381-29266382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533649977	chr22:29266413-29266414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373040749	chr22:29266440-29266441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556965416	chr22:29266456-29266457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560280699	chr22:29266479-29266480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527722837	chr22:29266589-29266590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549171562	chr22:29266629-29266630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375674776	chr22:29266641-29266642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs79223004	chr22:29266665-29266666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77771730	chr22:29266667-29266668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370046003	chr22:29266695-29266696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549583296	chr22:29266705-29266706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs118189807	chr22:29266734-29266735	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
low-grade B-cell lymphoma tumor	18367492	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
Cancer	21183584	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
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29261800-29265600	Weak transcription	Fetal Intestine Small	intestine
2	chr22:29262200-29265400	Weak transcription	Liver	Liver
3	chr22:29264000-29265200	Weak transcription	HepG2	liver
4	chr22:29265200-29266400	Enhancers	HepG2	liver
5	chr22:29265400-29266200	Enhancers	Liver	Liver
6	chr22:29265600-29266200	Enhancers	Fetal Intestine Small	intestine
7	chr22:29266200-29278400	Weak transcription	Fetal Intestine Small	intestine
8	chr22:29266400-29270800	Weak transcription	HepG2	liver
9	chr22:29269400-29269600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr22:29269400-29269800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr22:29269400-29270000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr22:29269400-29270000	Active TSS	Brain Angular Gyrus	brain
13	chr22:29269400-29271400	Enhancers	HSMMtube	muscle
14	chr22:29269600-29271200	Enhancers	Fetal Muscle Leg	muscle
15	chr22:29270200-29270400	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr22:29270800-29271200	Enhancers	HepG2	liver
17	chr22:29271200-29276000	Weak transcription	Fetal Muscle Leg	muscle
18	chr22:29271200-29276800	Weak transcription	HepG2	liver
19	chr22:29271400-29276000	Weak transcription	HSMMtube	muscle
20	chr22:29273600-29274000	Enhancers	Liver	Liver
21	chr22:29273600-29274200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr22:29273600-29274200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr22:29273600-29274800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr22:29273800-29274200	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr22:29274000-29274200	Enhancers	Stomach Mucosa	stomach
26	chr22:29274000-29278400	Weak transcription	Liver	Liver
27	chr22:29274200-29278400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr22:29274400-29275600	Weak transcription	Stomach Mucosa	stomach
29	chr22:29274800-29278400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr22:29275600-29276400	Enhancers	Fetal Heart	heart
31	chr22:29275600-29276400	Enhancers	Stomach Mucosa	stomach
32	chr22:29275800-29276600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr22:29276000-29276200	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr22:29276000-29276200	Enhancers	Brain Angular Gyrus	brain
35	chr22:29276000-29276600	Enhancers	HSMMtube	muscle
36	chr22:29276000-29276800	Enhancers	Fetal Muscle Leg	muscle
37	chr22:29276200-29278400	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr22:29276200-29278400	Weak transcription	Brain Angular Gyrus	brain
39	chr22:29276400-29276600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr22:29276400-29278200	Weak transcription	Fetal Heart	heart
41	chr22:29276400-29278400	Weak transcription	Stomach Mucosa	stomach
42	chr22:29276600-29276800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr22:29276600-29278400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr22:29276600-29278600	Weak transcription	HSMMtube	muscle
45	chr22:29276800-29278000	Weak transcription	Fetal Muscle Leg	muscle
46	chr22:29276800-29278400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr22:29276800-29278400	Enhancers	HepG2	liver
48	chr22:29277000-29277200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr22:29277200-29278600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr22:29277600-29277800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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