Variant report

Variant	esv17527
Chromosome Location	chr22:29066121-29102976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:535)
CpG islands
(count:549)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:535 , 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	chr22:29071147-29071157	K562	blood:	n/a	n/a
2	ATF1	chr22:29076933-29077144	K562	blood:	n/a	n/a
3	ATF2	chr22:29069985-29070415	GM12878	blood:	n/a	n/a
4	ATF3	chr22:29076874-29077103	K562	blood:	n/a	n/a
5	BACH1	chr22:29075695-29076206	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr22:29075339-29075367	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr22:29088557-29088776	GM12878	blood:	n/a	n/a
8	BATF	chr22:29072176-29072389	GM12878	blood:	n/a	n/a
9	BATF	chr22:29084039-29084373	GM12878	blood:	n/a	n/a
10	BATF	chr22:29088114-29088341	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:29085983-29086182	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:29070081-29070349	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:29076664-29076907	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:29079431-29079609	GM12878	blood:	n/a	n/a
15	BCL11A	chr22:29088139-29088370	GM12878	blood:	n/a	chr22:29088204-29088212
16	BCL11A	chr22:29072214-29072534	GM12878	blood:	n/a	n/a
17	BCL3	chr22:29070034-29070394	GM12878	blood:	n/a	n/a
18	BHLHE40	chr22:29076849-29076985	HepG2	liver:	n/a	n/a
19	BHLHE40	chr22:29076012-29076324	GM12878	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
20	BHLHE40	chr22:29075875-29076373	K562	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
21	BHLHE40	chr22:29075834-29076370	HepG2	liver:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
22	BHLHE40	chr22:29076134-29076273	A549	lung:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
23	BRCA1	chr22:29075353-29075356	GM12878	blood:	n/a	n/a
24	CBX3	chr22:29070039-29070343	K562	blood:	n/a	chr22:29070074-29070085
25	CCNT2	chr22:29075326-29075382	K562	blood:	n/a	n/a
26	CEBPB	chr22:29076791-29077162	HepG2	liver:	n/a	chr22:29076972-29076983
27	CEBPB	chr22:29076869-29077080	HepG2	liver:	n/a	chr22:29076972-29076983
28	CEBPB	chr22:29069964-29070527	GM12878	blood:	n/a	n/a
29	CEBPB	chr22:29076953-29076998	H1-hESC	embryonic stem cell:	n/a	chr22:29076972-29076983
30	CEBPB	chr22:29076766-29077109	K562	blood:	n/a	chr22:29076972-29076983
31	CEBPB	chr22:29076789-29077167	Hela-S3	cervix:	n/a	chr22:29076972-29076983
32	CEBPB	chr22:29076886-29077036	K562	blood:	n/a	chr22:29076972-29076983
33	CEBPB	chr22:29076904-29077084	HepG2	liver:	n/a	chr22:29076972-29076983
34	CEBPB	chr22:29076789-29077165	A549	lung:	n/a	chr22:29076972-29076983
35	CEBPB	chr22:29100786-29100969	HepG2	liver:	n/a	chr22:29100830-29100847 chr22:29100833-29100844
36	CEBPB	chr22:29076785-29077169	IMR90	lung:	n/a	chr22:29076972-29076983
37	CEBPB	chr22:29076789-29077168	HepG2	liver:	n/a	chr22:29076972-29076983
38	CEBPB	chr22:29076790-29077167	K562	blood:	n/a	chr22:29076972-29076983
39	CEBPD	chr22:29075821-29076234	HepG2	liver:	n/a	n/a
40	CHD2	chr22:29075341-29075521	K562	blood:	n/a	n/a
41	CHD2	chr22:29075282-29075552	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr22:29075618-29076123	HepG2	liver:	n/a	n/a
43	CREB1	chr22:29075608-29076170	A549	lung:	n/a	n/a
44	CTCF	chr22:29099580-29099730	HMF	breast:	n/a	n/a
45	CTCF	chr22:29075841-29075970	LNCaP	prostate:	n/a	n/a
46	CTCF	chr22:29075938-29075985	LNCaP	prostate:	n/a	n/a
47	CTCF	chr22:29075860-29075946	GM12891	blood:	n/a	n/a
48	CTCF	chr22:29068830-29068894	GM13977	blood:	n/a	n/a
49	CTCF	chr22:29078468-29078509	GM13976	blood:	n/a	n/a
50	CTCF	chr22:29080765-29080844	Lung_OC	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29076383-29076433	HIPEpiC	eye:	n/a
2	chr22:29078644-29078694	HNPCEpiC	eye:	n/a
3	chr22:29076113-29076163	K562	blood:	n/a
4	chr22:29072190-29072240	HCT-116	colon:	n/a
5	chr22:29075247-29075297	T-47D	breast:	n/a
6	chr22:29073496-29073546	SK-N-MC	brain:	n/a
7	chr22:29072190-29072240	PFSK-1	brain:	n/a
8	chr22:29072190-29072240	HCPEpiC	choroid plexus:	n/a
9	chr22:29073496-29073546	NH-A	brain:	n/a
10	chr22:29073496-29073546	A549	lung:	n/a
11	chr22:29076175-29076225	PrEC	prostate:	n/a
12	chr22:29076175-29076225	K562	blood:	n/a
13	chr22:29074955-29075005	Hepatocyte	liver:	n/a
14	chr22:29073496-29073546	AoSMC	blood vessel:	n/a
15	chr22:29072190-29072240	PANC-1	pancreas:	n/a
16	chr22:29073496-29073546	NHBE	bronchial:	n/a
17	chr22:29073496-29073546	MCF-7	breast:	n/a
18	chr22:29075159-29075209	HNPCEpiC	eye:	n/a
19	chr22:29074955-29075005	PrEC	prostate:	n/a
20	chr22:29078644-29078694	GM12892	blood:	n/a
21	chr22:29075159-29075209	SAEC	small airway:	n/a
22	chr22:29075247-29075297	HCF	heart:	n/a
23	chr22:29074955-29075005	NT2-D1	testis:	n/a
24	chr22:29075247-29075297	SK-N-MC	brain:	n/a
25	chr22:29074955-29075005	AG10803	skin:	n/a
26	chr22:29075247-29075297	GM12878	blood:	n/a
27	chr22:29075247-29075297	SK-N-SH_RA	brain:	n/a
28	chr22:29076113-29076163	NB4	blood:	n/a
29	chr22:29072190-29072240	HEEpiC	esophagus:	n/a
30	chr22:29076175-29076225	Caco-2	colon:	n/a
31	chr22:29078644-29078694	ECC-1	luminal epithelium:	n/a
32	chr22:29076175-29076225	AG04449	skin:	fetal
33	chr22:29076383-29076433	K562	blood:	n/a
34	chr22:29076383-29076433	LNCaP	prostate:	n/a
35	chr22:29076175-29076225	MCF10A-Er-Src	breast:	n/a
36	chr22:29075159-29075209	GM19239	blood:	n/a
37	chr22:29076175-29076225	HCT-116	colon:	n/a
38	chr22:29072190-29072240	NH-A	brain:	n/a
39	chr22:29076113-29076163	GM06990	blood:	n/a
40	chr22:29072190-29072240	NT2-D1	testis:	n/a
41	chr22:29074955-29075005	HL-60	blood:	n/a
42	chr22:29074955-29075005	Caco-2	colon:	n/a
43	chr22:29075159-29075209	HRPEpiC	eye:	n/a
44	chr22:29073496-29073546	MCF10A-Er-Src	breast:	n/a
45	chr22:29076175-29076225	CMK	blood:	n/a
46	chr22:29073496-29073546	T-47D	breast:	n/a
47	chr22:29072190-29072240	HRPEpiC	eye:	n/a
48	chr22:29076383-29076433	MCF-7	breast:	n/a
49	chr22:29072190-29072240	GM12892	blood:	n/a
50	chr22:29076175-29076225	PANC-1	pancreas:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29098955..29101024-chr22:29190318..29193070,2	K562	blood:
2	chr22:29094612..29096688-chr22:29136318..29138280,2	K562	blood:
3	chr22:29090716..29093047-chr22:29154418..29156765,2	K562	blood:
4	chr22:29065542..29067314-chr3:70716964..70718547,2	MCF-7	breast:
5	chr22:29068475..29070803-chr22:29136306..29139155,2	K562	blood:
6	chr22:29093925..29096043-chr22:29097734..29099299,2	K562	blood:
7	chr22:29068301..29072007-chr22:29167336..29171119,3	K562	blood:
8	chr22:29069948..29071525-chr22:29073386..29075260,2	K562	blood:
9	chr22:29054009..29055541-chr22:29066036..29068259,2	K562	blood:
10	chr22:29069948..29071525-chr22:29073386..29075260,2	K562	blood:
11	chr22:29074345..29076106-chr22:29137826..29140000,2	K562	blood:
12	chr22:29065798..29067377-chr22:29180206..29181854,2	MCF-7	breast:
13	chr22:29051030..29053991-chr22:29069549..29071319,2	K562	blood:
14	chr22:29098731..29101679-chr22:29195064..29196979,2	MCF-7	breast:
15	chr22:29093925..29096043-chr22:29097734..29099299,2	K562	blood:
16	chr22:29071306..29073725-chr22:29073922..29075807,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC28-1	chr22:29085123-29085398	NONHSAT084651
2	lnc-TTC28-1	chr22:29083737-29083974	NONHSAT084651

No data

Variant related genes	Relation type
CHEK2	TF binding region
TTC28	TF binding region
CHEK2	CpG island
TTC28	CpG island
ENSG00000226471	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000183765	chromatin interactions
ENSG00000100154	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000159873	chromatin interactions

Extended variants
information (count: 1616 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9613662	chr22:29066195-29066196	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577334864	chr22:29066197-29066198	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564727004	chr22:29066222-29066223	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143947588	chr22:29066272-29066273	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575745275	chr22:29066345-29066346	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546176074	chr22:29066364-29066365	ZNF genes & repeats Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561442426	chr22:29066451-29066452	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562982025	chr22:29066460-29066461	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544673905	chr22:29066525-29066526	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs118181016	chr22:29066568-29066569	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139398215	chr22:29066598-29066599	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550169965	chr22:29066653-29066654	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201625635	chr22:29066669-29066670	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564739231	chr22:29066682-29066683	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs202067472	chr22:29066692-29066693	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149278914	chr22:29066693-29066694	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533279344	chr22:29066702-29066703	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146863439	chr22:29066724-29066725	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78566588	chr22:29066747-29066748	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566694160	chr22:29066776-29066777	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75766087	chr22:29066857-29066858	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188156369	chr22:29066900-29066901	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547163099	chr22:29066925-29066926	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192681196	chr22:29066939-29066940	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535913563	chr22:29066965-29066966	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562173625	chr22:29067037-29067038	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182698767	chr22:29067086-29067087	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561312370	chr22:29067105-29067106	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs118037283	chr22:29067122-29067123	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140669117	chr22:29067139-29067140	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9620812	chr22:29067199-29067200	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558142774	chr22:29067229-29067230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573428321	chr22:29067234-29067235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540415285	chr22:29067249-29067250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547791082	chr22:29067252-29067253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187797148	chr22:29067297-29067298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150446509	chr22:29067346-29067347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562518877	chr22:29067349-29067350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532774262	chr22:29067419-29067420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545314274	chr22:29067420-29067421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560185585	chr22:29067490-29067491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377735999	chr22:29067492-29067493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527523400	chr22:29067547-29067548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549211265	chr22:29067548-29067549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76205402	chr22:29067578-29067579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13058196	chr22:29067620-29067621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370262568	chr22:29067622-29067623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565340574	chr22:29067623-29067624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371933646	chr22:29067652-29067653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374970721	chr22:29067670-29067671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20616022	CNVD
Breast cancer	21486468	CNVD
Ovarian cancer	21486468	CNVD

Chromatin state (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29046400-29073800	Weak transcription	Ovary	ovary
2	chr22:29052600-29074600	Weak transcription	Colon Smooth Muscle	Colon
3	chr22:29053400-29066800	Weak transcription	Fetal Lung	lung
4	chr22:29056800-29074600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr22:29057600-29070200	Weak transcription	Fetal Stomach	stomach
6	chr22:29058000-29070200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr22:29064600-29074800	Weak transcription	Left Ventricle	heart
8	chr22:29064800-29069800	Weak transcription	HUVEC	blood vessel
9	chr22:29065600-29067000	Enhancers	NHDF-Ad	bronchial
10	chr22:29065800-29066400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
11	chr22:29065800-29067200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr22:29066200-29066400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
13	chr22:29066800-29067000	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
14	chr22:29066800-29067000	ZNF genes & repeats	Fetal Lung	lung
15	chr22:29066800-29067200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr22:29066800-29067200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr22:29066800-29067200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr22:29067000-29069400	Weak transcription	NHDF-Ad	bronchial
19	chr22:29067000-29069800	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr22:29067000-29074400	Weak transcription	Fetal Lung	lung
21	chr22:29067200-29068600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:29067200-29068600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr22:29067200-29073800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr22:29067200-29074400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr22:29067400-29069600	Weak transcription	Fetal Muscle Leg	muscle
26	chr22:29067600-29074400	Weak transcription	Fetal Brain Female	brain
27	chr22:29067800-29074400	Weak transcription	HepG2	liver
28	chr22:29068400-29068600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
29	chr22:29068600-29068800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr22:29068600-29069600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr22:29068600-29069800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr22:29068600-29069800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
33	chr22:29068800-29069000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr22:29068800-29069200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
35	chr22:29068800-29069400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr22:29068800-29069800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
37	chr22:29068800-29069800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr22:29068800-29070800	Bivalent Enhancer	Dnd41	blood
39	chr22:29068800-29071400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
40	chr22:29068800-29071400	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
41	chr22:29068800-29071400	Enhancers	GM12878-XiMat	blood
42	chr22:29069000-29069400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr22:29069000-29069600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
44	chr22:29069200-29069400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr22:29069200-29071000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr22:29069400-29069600	Bivalent Enhancer	Primary B cells from cord blood	blood
47	chr22:29069400-29069600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
48	chr22:29069400-29069600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
49	chr22:29069400-29069600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr22:29069400-29069600	Enhancers	NHDF-Ad	bronchial

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