Variant report

Variant	esv1833221
Chromosome Location	chr22:30274129-30297376
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	BACH1	chr22:30279479-30279812	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr22:30279600-30279919	GM12878	blood:	n/a	n/a
3	BHLHE40	chr22:30279106-30279791	K562	blood:	n/a	chr22:30279511-30279527
4	BHLHE40	chr22:30278918-30279151	GM12878	blood:	n/a	chr22:30279006-30279022 chr22:30279105-30279121
5	BRCA1	chr22:30279422-30279568	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr22:30279225-30279344	GM12878	blood:	n/a	n/a
7	BRCA1	chr22:30279281-30279298	HepG2	liver:	n/a	n/a
8	CCNT2	chr22:30278996-30279811	K562	blood:	n/a	chr22:30279052-30279061 chr22:30279470-30279479
9	CEBPB	chr22:30291550-30291641	K562	blood:	n/a	chr22:30291581-30291592
10	CEBPB	chr22:30282656-30282856	HepG2	liver:	n/a	n/a
11	CEBPB	chr22:30297362-30297676	K562	blood:	n/a	n/a
12	CEBPB	chr22:30297366-30297631	K562	blood:	n/a	n/a
13	CEBPB	chr22:30282643-30282930	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr22:30279056-30279292	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr22:30291559-30291624	HepG2	liver:	n/a	chr22:30291581-30291592
16	CHD1	chr22:30279159-30279853	GM12878	blood:	n/a	chr22:30279597-30279607
17	CHD2	chr22:30279277-30279413	K562	blood:	n/a	n/a
18	CHD2	chr22:30279008-30279955	GM12878	blood:	n/a	chr22:30279597-30279607
19	CHD2	chr22:30279226-30279565	HepG2	liver:	n/a	n/a
20	CHD2	chr22:30278968-30279791	Hela-S3	cervix:	n/a	chr22:30279597-30279607
21	CHD2	chr22:30275813-30276023	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr22:30279307-30279629	A549	lung:	n/a	n/a
23	CTCF	chr22:30279460-30279610	AG04450	lung:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
24	CTCF	chr22:30279580-30279730	AG10803	skin:	n/a	n/a
25	CTCF	chr22:30279420-30279570	NHDF-neo	bronchial:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
26	CTCF	chr22:30279540-30279690	K562	blood:	n/a	n/a
27	CTCF	chr22:30279723-30279729	A549	lung:	n/a	n/a
28	CTCF	chr22:30279440-30279590	WI-38	lung:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
29	CTCF	chr22:30279460-30279610	BE2_C	brain:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
30	CTCF	chr22:30279451-30279593	LNCaP	prostate:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
31	CTCF	chr22:30279500-30279650	HCM	heart:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
32	CTCF	chr22:30279480-30279630	MCF-7	breast:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
33	CTCF	chr22:30279351-30279892	K562	blood:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
34	CTCF	chr22:30279342-30279901	IMR90	lung:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
35	CTCF	chr22:30279460-30279610	HA-sp	spinal cord:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
36	CTCF	chr22:30279360-30279510	BE2_C	brain:	n/a	n/a
37	CTCF	chr22:30279440-30279522	GM13977	blood:	n/a	n/a
38	CTCF	chr22:30279700-30279850	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr22:30279684-30279782	GM13977	blood:	n/a	n/a
40	CTCF	chr22:30279440-30279590	AG04449	skin:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
41	CTCF	chr22:30279720-30279870	HCFaa	heart:	n/a	n/a
42	CTCF	chr22:30279450-30279517	GM10248	blood:	n/a	n/a
43	CTCF	chr22:30279449-30279569	Lung_OC	lung:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
44	CTCF	chr22:30279440-30279590	SK-N-SH_RA	brain:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
45	CTCF	chr22:30279440-30279590	GM12873	blood:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
46	CTCF	chr22:30279400-30279550	GM12869	blood:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
47	CTCF	chr22:30279440-30279590	HPAF	blood vessel:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
48	CTCF	chr22:30279440-30279590	AG09319	gingival:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
49	CTCF	chr22:30279357-30279568	Kidney_OC	kidney:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
50	CTCF	chr22:30279448-30279584	MCF-7	breast:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30278994-30279044	MCF10A-Er-Src	breast:	n/a
2	chr22:30279318-30279368	HMEC	breast:	n/a
3	chr22:30278994-30279044	MCF10A-Er-Src	breast:	n/a
4	chr22:30279318-30279368	HMEC	breast:	n/a
5	chr22:30283578-30283628	NHDF-neo	bronchial:	n/a
6	chr22:30279241-30279291	BE2_C	brain:	n/a
7	chr22:30283578-30283628	AG09319	gingival:	n/a
8	chr22:30278994-30279044	PFSK-1	brain:	n/a
9	chr22:30278994-30279044	NHDF-neo	bronchial:	n/a
10	chr22:30275268-30275318	U87	brain:	n/a
11	chr22:30279922-30279972	HEK293	kidney:	embryo
12	chr22:30278876-30278926	ProgFib	skin:	n/a
13	chr22:30275268-30275318	PFSK-1	brain:	n/a
14	chr22:30277968-30278018	HPAEpiC	pulmonary alveolar:	n/a
15	chr22:30275268-30275318	GM19239	blood:	n/a
16	chr22:30277968-30278018	ECC-1	luminal epithelium:	n/a
17	chr22:30279922-30279972	MCF-7	breast:	n/a
18	chr22:30275268-30275318	GM12891	blood:	n/a
19	chr22:30278994-30279044	GM12891	blood:	n/a
20	chr22:30278994-30279044	Hepatocyte	liver:	n/a
21	chr22:30279318-30279368	HEEpiC	esophagus:	n/a
22	chr22:30277968-30278018	GM06990	blood:	n/a
23	chr22:30275268-30275318	NH-A	brain:	n/a
24	chr22:30279922-30279972	GM12892	blood:	n/a
25	chr22:30283578-30283628	IMR90	lung:	fetal
26	chr22:30278876-30278926	HepG2	liver:	n/a
27	chr22:30278992-30279042	GM12892	blood:	n/a
28	chr22:30277391-30277441	HCM	heart:	n/a
29	chr22:30279857-30279907	Caco-2	colon:	n/a
30	chr22:30275268-30275318	MCF10A-Er-Src	breast:	n/a
31	chr22:30277391-30277441	HL-60	blood:	n/a
32	chr22:30278994-30279044	SAEC	small airway:	n/a
33	chr22:30278876-30278926	CMK	blood:	n/a
34	chr22:30278994-30279044	SKMC	muscle:	n/a
35	chr22:30278994-30279044	HCPEpiC	choroid plexus:	n/a
36	chr22:30277391-30277441	NH-A	brain:	n/a
37	chr22:30283578-30283628	HRPEpiC	eye:	n/a
38	chr22:30279922-30279972	BJ	skin:	n/a
39	chr22:30279241-30279291	Jurkat	blood:	n/a
40	chr22:30278876-30278926	GM12878	blood:	n/a
41	chr22:30279318-30279368	Caco-2	colon:	n/a
42	chr22:30279857-30279907	SK-N-MC	brain:	n/a
43	chr22:30277968-30278018	LNCaP	prostate:	n/a
44	chr22:30279922-30279972	Hepatocyte	liver:	n/a
45	chr22:30279318-30279368	HCF	heart:	n/a
46	chr22:30278876-30278926	Hela-S3	cervix:	n/a
47	chr22:30278876-30278926	RPTEC	kidney:	n/a
48	chr22:30277391-30277441	GM19239	blood:	n/a
49	chr22:30277968-30278018	A549	lung:	n/a
50	chr22:30278992-30279042	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:30208243..30210090-chr22:30279066..30280884,2	MCF-7	breast:
2	chr22:30267624..30270362-chr22:30273098..30276358,3	K562	blood:
3	chr10:62193967..62194535-chr22:30279507..30280085,2	MCF-7	breast:
4	chr22:30288615..30290652-chr22:30302494..30304851,2	MCF-7	breast:
5	chr22:30265481..30267590-chr22:30272869..30274738,2	MCF-7	breast:
6	chr22:30229506..30231085-chr22:30279535..30281040,2	MCF-7	breast:
7	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
8	chr22:30289517..30291568-chr22:30301427..30303381,2	K562	blood:
9	chr22:30277721..30280339-chr22:30399364..30402748,3	K562	blood:
10	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
11	chr22:30232954..30235817-chr22:30277750..30279574,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HORMAD2-6	chr22:30279168-30279348	NONHSAT084740

Variant related genes	Relation type
RNU6-331P	TF binding region
MTMR3	TF binding region
RNU6-331P	CpG island
MTMR3	CpG island
ENSG00000100325	chromatin interactions
ENSG00000100330	chromatin interactions

Extended variants
information (count: 919 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537733254	chr22:30274169-30274170	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs147252348	chr22:30274185-30274186	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs552342788	chr22:30274199-30274200	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs73394887	chr22:30274231-30274232	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs139018086	chr22:30274239-30274240	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs553157817	chr22:30274262-30274263	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs80004216	chr22:30274275-30274276	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs9614094	chr22:30274301-30274302	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs28520101	chr22:30274324-30274325	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs5752975	chr22:30274335-30274336	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs575517255	chr22:30274356-30274357	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs546202375	chr22:30274360-30274361	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs555271200	chr22:30274412-30274413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564181666	chr22:30274416-30274417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs5844880	chr22:30274423-30274424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530027844	chr22:30274424-30274425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1968072	chr22:30274426-30274427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79608846	chr22:30274427-30274428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201599927	chr22:30274439-30274440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369939961	chr22:30274452-30274453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540420530	chr22:30274476-30274477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561912186	chr22:30274535-30274536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528976922	chr22:30274541-30274542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575172261	chr22:30274568-30274569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187037483	chr22:30274577-30274578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550727836	chr22:30274582-30274583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562618396	chr22:30274603-30274604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191071398	chr22:30274615-30274616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551360169	chr22:30274636-30274637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571013386	chr22:30274641-30274642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535022282	chr22:30274673-30274674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546784515	chr22:30274707-30274708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150587438	chr22:30274714-30274715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112487185	chr22:30274721-30274722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557149452	chr22:30274731-30274732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149722453	chr22:30274770-30274771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533635462	chr22:30274774-30274775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146233298	chr22:30274808-30274809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113881885	chr22:30274836-30274837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117685112	chr22:30274853-30274854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182457945	chr22:30274863-30274864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553801510	chr22:30274984-30274985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9620926	chr22:30275091-30275092	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs573845165	chr22:30275155-30275156	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs28595572	chr22:30275168-30275169	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs562396484	chr22:30275176-30275177	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs12169015	chr22:30275249-30275250	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs551077663	chr22:30275261-30275262	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs189682130	chr22:30275282-30275283	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs528735880	chr22:30275289-30275290	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	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
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30268800-30277800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr22:30268800-30279000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr22:30269000-30278800	Weak transcription	Adipose Nuclei	Adipose
4	chr22:30270200-30279200	Weak transcription	Spleen	Spleen
5	chr22:30273400-30274400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr22:30273600-30274400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr22:30273600-30274400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr22:30273600-30274400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr22:30273600-30274400	Bivalent Enhancer	NHDF-Ad	bronchial
10	chr22:30273800-30274200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr22:30273800-30274200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr22:30273800-30274200	Enhancers	HSMMtube	muscle
13	chr22:30273800-30274200	Flanking Active TSS	Osteobl	bone
14	chr22:30273800-30274400	Enhancers	Muscle Satellite Cultured Cells	--
15	chr22:30273800-30274400	Enhancers	HSMM	muscle
16	chr22:30274000-30278800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr22:30274200-30274400	Enhancers	Osteobl	bone
18	chr22:30274400-30275800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr22:30274400-30278800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr22:30277400-30278800	Enhancers	HepG2	liver
21	chr22:30277800-30278600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr22:30278200-30278400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr22:30278400-30278600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr22:30278400-30278800	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr22:30278400-30278800	Enhancers	Primary B cells from cord blood	blood
26	chr22:30278400-30278800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr22:30278400-30278800	Enhancers	Brain Anterior Caudate	brain
28	chr22:30278400-30278800	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr22:30278400-30279200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr22:30278400-30279200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr22:30278600-30278800	Enhancers	Primary B cells from peripheral blood	blood
32	chr22:30278600-30278800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr22:30278600-30278800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr22:30278600-30278800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr22:30278600-30278800	Enhancers	Dnd41	blood
36	chr22:30278600-30278800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr22:30278600-30279000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr22:30278600-30279000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr22:30278600-30279200	Active TSS	Brain Germinal Matrix	brain
40	chr22:30278600-30279800	Active TSS	Primary T cells from cord blood	blood
41	chr22:30278600-30279800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr22:30278600-30280000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr22:30278600-30280200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr22:30278600-30280400	Active TSS	Fetal Kidney	kidney
45	chr22:30278600-30280600	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr22:30278600-30280600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr22:30278600-30280600	Active TSS	Fetal Brain Female	brain
48	chr22:30278600-30281400	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr22:30278800-30279000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr22:30278800-30279000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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