Variant report

Variant	nsv1067544
Chromosome Location	chr22:28755418-29055246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1959)
CpG islands
(count:367)
Chromatin interactive
region (count:86)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1959 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:28770013-28770144	K562	blood:	n/a	n/a
2	ARID3A	chr22:28820669-28821181	HepG2	liver:	n/a	chr22:28821096-28821112
3	ARID3A	chr22:29025583-29025707	K562	blood:	n/a	n/a
4	ARID3A	chr22:28940311-28941057	K562	blood:	n/a	n/a
5	ARID3A	chr22:28762794-28763285	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:28963176-28963435	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:28791636-28792362	HepG2	liver:	n/a	n/a
8	ARID3A	chr22:28953316-28953439	K562	blood:	n/a	n/a
9	ARID3A	chr22:28996496-28996921	K562	blood:	n/a	n/a
10	ARID3A	chr22:28841013-28841073	K562	blood:	n/a	n/a
11	ARID3A	chr22:28791829-28792390	K562	blood:	n/a	n/a
12	ARID3A	chr22:28956042-28956807	K562	blood:	n/a	n/a
13	ARID3A	chr22:29006059-29006199	K562	blood:	n/a	n/a
14	ARID3A	chr22:28837580-28838572	HepG2	liver:	n/a	n/a
15	ARID3A	chr22:28996568-28996914	HepG2	liver:	n/a	n/a
16	ARID3A	chr22:28990734-28991082	HepG2	liver:	n/a	n/a
17	ARID3A	chr22:28822881-28822955	K562	blood:	n/a	n/a
18	ARID3A	chr22:28839621-28839801	K562	blood:	n/a	n/a
19	ARID3A	chr22:28838144-28838439	K562	blood:	n/a	n/a
20	ATF1	chr22:28780498-28780647	K562	blood:	n/a	n/a
21	ATF1	chr22:28858144-28858452	K562	blood:	n/a	n/a
22	ATF1	chr22:28797122-28797285	K562	blood:	n/a	n/a
23	ATF1	chr22:29025435-29025750	K562	blood:	n/a	n/a
24	ATF1	chr22:28955997-28956765	K562	blood:	n/a	n/a
25	ATF1	chr22:28792125-28792317	K562	blood:	n/a	n/a
26	ATF1	chr22:28990731-28990957	K562	blood:	n/a	n/a
27	ATF1	chr22:28940460-28940801	K562	blood:	n/a	n/a
28	ATF1	chr22:28806113-28806747	K562	blood:	n/a	n/a
29	ATF2	chr22:28806444-28806741	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr22:28806314-28806778	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr22:29023827-29024138	K562	blood:	n/a	n/a
32	ATF3	chr22:28956287-28956722	K562	blood:	n/a	n/a
33	ATF3	chr22:29025463-29025700	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr22:28806432-28806692	K562	blood:	n/a	n/a
35	ATF3	chr22:29025361-29025756	K562	blood:	n/a	n/a
36	ATF3	chr22:29025377-29025847	HCT-116	colon:	n/a	n/a
37	BACH1	chr22:28775128-28775395	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr22:28775120-28775437	K562	blood:	n/a	n/a
39	BACH1	chr22:28839475-28839800	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr22:28838196-28839029	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr22:28792819-28792907	K562	blood:	n/a	n/a
42	BACH1	chr22:29025970-29026088	H1-hESC	embryonic stem cell:	n/a	n/a
43	BATF	chr22:28798588-28798836	GM12878	blood:	n/a	n/a
44	BATF	chr22:28884270-28884439	GM12878	blood:	n/a	n/a
45	BCL3	chr22:28820635-28821169	A549	lung:	n/a	n/a
46	BHLHE40	chr22:28820720-28821039	HepG2	liver:	n/a	n/a
47	BHLHE40	chr22:28838138-28838658	K562	blood:	n/a	n/a
48	BHLHE40	chr22:28990782-28990977	GM12878	blood:	n/a	n/a
49	BHLHE40	chr22:28838233-28838573	GM12878	blood:	n/a	n/a
50	BHLHE40	chr22:29052245-29052411	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:28838631-28838681	SAEC	small airway:	n/a
2	chr22:28838631-28838681	SAEC	small airway:	n/a
3	chr22:28839137-28839187	PrEC	prostate:	n/a
4	chr22:28839667-28839717	RPTEC	kidney:	n/a
5	chr22:28839667-28839717	LNCaP	prostate:	n/a
6	chr22:28838631-28838681	NT2-D1	testis:	n/a
7	chr22:28838019-28838069	AG09309	skin:	n/a
8	chr22:28839667-28839717	HepG2	liver:	n/a
9	chr22:28838631-28838681	NB4	blood:	n/a
10	chr22:28839249-28839299	AG04450	lung:	fetal
11	chr22:28839137-28839187	HPAEpiC	pulmonary alveolar:	n/a
12	chr22:28839667-28839717	PrEC	prostate:	n/a
13	chr22:28838019-28838069	PANC-1	pancreas:	n/a
14	chr22:28838019-28838069	AG10803	skin:	n/a
15	chr22:28839249-28839299	RPTEC	kidney:	n/a
16	chr22:28839249-28839299	HPAEpiC	pulmonary alveolar:	n/a
17	chr22:28838019-28838069	Jurkat	blood:	n/a
18	chr22:28839667-28839717	NB4	blood:	n/a
19	chr22:28839667-28839717	NHBE	bronchial:	n/a
20	chr22:28839137-28839187	SAEC	small airway:	n/a
21	chr22:28839667-28839717	Hela-S3	cervix:	n/a
22	chr22:28839137-28839187	MCF-7	breast:	n/a
23	chr22:28837586-28837636	SK-N-SH	brain:	n/a
24	chr22:28839249-28839299	A549	lung:	n/a
25	chr22:28838019-28838069	BJ	skin:	n/a
26	chr22:28839249-28839299	ovcar-3	ovarian:	n/a
27	chr22:28839137-28839187	MCF10A-Er-Src	breast:	n/a
28	chr22:28839137-28839187	GM12892	blood:	n/a
29	chr22:28839249-28839299	GM12892	blood:	n/a
30	chr22:28839249-28839299	PFSK-1	brain:	n/a
31	chr22:28839137-28839187	HUVEC	blood vessel:	n/a
32	chr22:28839137-28839187	HCF	heart:	n/a
33	chr22:28839137-28839187	AG10803	skin:	n/a
34	chr22:28839249-28839299	ProgFib	skin:	n/a
35	chr22:28839249-28839299	CMK	blood:	n/a
36	chr22:28839667-28839717	T-47D	breast:	n/a
37	chr22:28839249-28839299	HCM	heart:	n/a
38	chr22:28838019-28838069	HRE	kidney:	n/a
39	chr22:28837586-28837636	BE2_C	brain:	n/a
40	chr22:28838631-28838681	PANC-1	pancreas:	n/a
41	chr22:28837586-28837636	LNCaP	prostate:	n/a
42	chr22:28838631-28838681	HRCEpiC	kidney:	n/a
43	chr22:28839137-28839187	PANC-1	pancreas:	n/a
44	chr22:28837586-28837636	H1-hESC	embryonic stem cell:	embryo
45	chr22:28838019-28838069	HAEpiC	amniotic membrane:	n/a
46	chr22:28839249-28839299	Jurkat	blood:	n/a
47	chr22:28839137-28839187	CMK	blood:	n/a
48	chr22:28839249-28839299	HCF	heart:	n/a
49	chr22:28839137-28839187	ECC-1	luminal epithelium:	n/a
50	chr22:28837586-28837636	ProgFib	skin:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:28959390..28962163-chr22:28964254..28967169,3	K562	blood:
2	chr22:28828789..28831593-chr22:28834204..28836919,2	K562	blood:
3	chr22:28951733..28954395-chr22:28960570..28962204,2	K562	blood:
4	chr22:28873207..28875970-chr22:28979240..28981638,2	K562	blood:
5	chr22:28886881..28888518-chr22:28890275..28892164,2	K562	blood:
6	chr22:28835448..28837338-chr22:28837546..28840029,2	MCF-7	breast:
7	chr22:29032416..29034687-chr22:29214164..29215890,2	MCF-7	breast:
8	chr22:28934195..28936559-chr22:28940613..28943481,2	K562	blood:
9	chr22:28789197..28789697-chr8:43093984..43094906,2	HCT-116	colon:
10	chr22:28857007..28859813-chr22:28867986..28869532,2	K562	blood:
11	chr22:29002103..29004832-chr22:29188346..29190789,2	MCF-7	breast:
12	chr22:28508644..28509412-chr22:28838027..28838971,3	MCF-7	breast:
13	chr22:28996345..28997098-chr22:29436390..29436927,2	K562	blood:
14	chr22:28396428..28399039-chr22:28886798..28889695,2	MCF-7	breast:
15	chr22:28847241..28850416-chr22:28850940..28854599,3	K562	blood:
16	chr22:29010223..29011832-chr22:29028588..29030915,2	K562	blood:
17	chr22:28995746..28997516-chr22:29186158..29188253,2	MCF-7	breast:
18	chr22:28416092..28416754-chr22:28837943..28838869,2	K562	blood:
19	chr22:28996270..28996801-chr22:29225446..29225968,2	MCF-7	breast:
20	chr22:28989732..28992397-chr22:28995428..28996933,2	K562	blood:
21	chr22:28986053..28988845-chr22:29188910..29191071,2	K562	blood:
22	chr22:29032998..29035850-chr22:29036079..29038084,2	MCF-7	breast:
23	chr22:28649021..28649823-chr22:28990464..28991307,3	MCF-7	breast:
24	chr22:28987741..28989762-chr22:29021256..29024194,2	K562	blood:
25	chr22:29010223..29011832-chr22:29028588..29030915,2	K562	blood:
26	chr22:28987741..28989762-chr22:29021256..29024194,2	K562	blood:
27	chr22:28828789..28831593-chr22:28834204..28836919,2	K562	blood:
28	chr22:28997050..28999545-chr22:28999902..29002703,2	MCF-7	breast:
29	chr22:28995898..28998203-chr22:29197005..29199575,2	K562	blood:
30	chr22:28822807..28825089-chr22:28828266..28830799,2	MCF-7	breast:
31	chr22:28996007..28999960-chr22:29194026..29197947,6	MCF-7	breast:
32	chr22:28799731..28802311-chr22:28804363..28806927,2	MCF-7	breast:
33	chr22:28946345..28949286-chr22:28954414..28956604,2	K562	blood:
34	chr22:29044552..29046919-chr22:29194055..29197686,3	K562	blood:
35	chr22:28415730..28416730-chr22:28990429..28991381,8	MCF-7	breast:
36	chr22:28995974..28997136-chr22:29225078..29225924,5	K562	blood:
37	chr22:28868844..28871454-chr22:28874181..28875792,2	K562	blood:
38	chr22:28447496..28448401-chr22:28837962..28838861,4	MCF-7	breast:
39	chr22:28447447..28448524-chr22:28837980..28838886,4	K562	blood:
40	chr22:29009654..29012223-chr22:29227592..29229292,2	K562	blood:
41	chr22:29032998..29035850-chr22:29036079..29038084,2	MCF-7	breast:
42	chr22:28447530..28448237-chr22:28837942..28838802,2	MCF-7	breast:
43	chr22:29054009..29055541-chr22:29066036..29068259,2	K562	blood:
44	chr22:28997050..28999545-chr22:28999902..29002703,2	MCF-7	breast:
45	chr22:28912407..28915228-chr22:28919764..28921704,2	K562	blood:
46	chr22:28994581..28996472-chr22:29204269..29206724,2	MCF-7	breast:
47	chr22:28888582..28890420-chr22:28895245..28897649,2	K562	blood:
48	chr22:28789180..28790711-chr22:28793203..28795069,2	MCF-7	breast:
49	chr22:28994240..28996811-chr22:29193296..29195303,2	MCF-7	breast:
50	chr22:29001462..29003738-chr22:29195242..29198224,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHEK2-1	chr22:29038969-29039258	NONHSAT084650

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5739	chr22:28855913-28855932	MIMAT0023116

No data

Variant related genes	Relation type
RN7SL162P	TF binding region
TTC28	TF binding region
RN7SL162P	CpG island
TTC28	CpG island
ENSG00000100154	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000266503	chromatin interactions

Extended variants
information (count: 9647 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:9647 , 50 per page) page: 1 2 3 4 5 6 7 ... 193

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185317798	chr22:28755448-28755449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs134509	chr22:28755545-28755546	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs74658247	chr22:28755628-28755629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78485278	chr22:28755630-28755631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577374565	chr22:28755646-28755647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116900803	chr22:28755733-28755734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553051095	chr22:28755746-28755747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568133327	chr22:28755782-28755783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574619974	chr22:28755785-28755786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541925570	chr22:28755811-28755812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188911474	chr22:28755853-28755854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192679990	chr22:28755887-28755888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530511374	chr22:28755889-28755890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546127734	chr22:28755898-28755899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564177711	chr22:28755930-28755931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528310588	chr22:28755948-28755949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112786928	chr22:28756011-28756012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs134510	chr22:28756039-28756040	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs149471461	chr22:28756116-28756117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530159857	chr22:28756171-28756172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs144790655	chr22:28756192-28756193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574906899	chr22:28756255-28756256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569754510	chr22:28756277-28756278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560160145	chr22:28756280-28756281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559227600	chr22:28756374-28756375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs117532770	chr22:28756382-28756383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184710196	chr22:28756431-28756432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375740545	chr22:28756483-28756484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556748214	chr22:28756512-28756513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576537439	chr22:28756516-28756517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575084848	chr22:28756517-28756518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541987131	chr22:28756555-28756556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs5762567	chr22:28756567-28756568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189163981	chr22:28756579-28756580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs738199	chr22:28756581-28756582	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs545453620	chr22:28756607-28756608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180908177	chr22:28756635-28756636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377683288	chr22:28756660-28756661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553207806	chr22:28756696-28756697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79107	chr22:28756710-28756711	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs540495896	chr22:28756767-28756768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532930492	chr22:28756779-28756780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540312153	chr22:28756797-28756798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185968861	chr22:28756798-28756799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529042414	chr22:28756836-28756837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111379997	chr22:28756862-28756863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141931645	chr22:28756873-28756874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374897439	chr22:28756881-28756882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572078377	chr22:28756894-28756895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148131012	chr22:28756903-28756904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:2520 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:28741600-28759000	Weak transcription	Fetal Stomach	stomach
2	chr22:28742800-28759600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr22:28743000-28759000	Weak transcription	Dnd41	blood
4	chr22:28748000-28755800	Weak transcription	Fetal Intestine Small	intestine
5	chr22:28748000-28759600	Weak transcription	Fetal Lung	lung
6	chr22:28752800-28759000	Weak transcription	Ovary	ovary
7	chr22:28752800-28768600	Weak transcription	Left Ventricle	heart
8	chr22:28754000-28759400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr22:28754200-28755800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr22:28754200-28755800	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr22:28754200-28756200	Enhancers	Fetal Brain Male	brain
12	chr22:28754400-28759200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr22:28754600-28757200	Weak transcription	Fetal Kidney	kidney
14	chr22:28754600-28759200	Weak transcription	Adipose Nuclei	Adipose
15	chr22:28754800-28755800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr22:28754800-28757400	Weak transcription	Fetal Heart	heart
17	chr22:28754800-28766000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr22:28755000-28755600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr22:28755000-28755600	Weak transcription	Right Ventricle	heart
20	chr22:28755000-28758000	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr22:28755000-28759200	Weak transcription	Psoas Muscle	Psoas
22	chr22:28755600-28755800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr22:28755600-28755800	Enhancers	Right Ventricle	heart
24	chr22:28755800-28757400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr22:28755800-28759200	Weak transcription	Right Ventricle	heart
26	chr22:28755800-28759400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr22:28756600-28759000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr22:28757000-28757800	Enhancers	Duodenum Mucosa	Duodenum
29	chr22:28757400-28757600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr22:28757600-28758200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr22:28758200-28759200	Weak transcription	Fetal Brain Female	brain
32	chr22:28759000-28759600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr22:28759000-28759800	ZNF genes & repeats	Fetal Stomach	stomach
34	chr22:28759000-28760200	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr22:28759000-28761800	ZNF genes & repeats	Dnd41	blood
36	chr22:28759200-28759400	ZNF genes & repeats	Fetal Brain Female	brain
37	chr22:28759200-28759600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr22:28759200-28759800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr22:28759200-28760000	Enhancers	Adipose Nuclei	Adipose
40	chr22:28759200-28760000	Enhancers	Psoas Muscle	Psoas
41	chr22:28759200-28760000	Enhancers	Right Ventricle	heart
42	chr22:28759600-28759800	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr22:28759600-28760000	ZNF genes & repeats	Fetal Lung	lung
44	chr22:28759600-28760000	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr22:28759600-28763600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr22:28759800-28766000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr22:28759800-28777200	Weak transcription	Fetal Stomach	stomach
48	chr22:28760000-28760200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr22:28760000-28761200	Weak transcription	Adipose Nuclei	Adipose
50	chr22:28760000-28766000	Weak transcription	Psoas Muscle	Psoas

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