Variant report

Variant	nsv914958
Chromosome Location	chr22:29586058-29620599
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1388)
CpG islands
(count:794)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1388 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29591655-29591957	K562	blood:	n/a	n/a
2	ATF1	chr22:29591528-29591943	K562	blood:	n/a	n/a
3	ATF1	chr22:29593118-29593369	K562	blood:	n/a	n/a
4	ATF2	chr22:29598302-29599397	GM12878	blood:	n/a	n/a
5	ATF2	chr22:29598245-29599384	GM12878	blood:	n/a	n/a
6	ATF3	chr22:29588553-29588763	K562	blood:	n/a	n/a
7	ATF3	chr22:29593069-29593342	K562	blood:	n/a	n/a
8	BACH1	chr22:29602255-29602337	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr22:29598729-29599005	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr22:29598215-29598576	GM12878	blood:	n/a	n/a
11	BATF	chr22:29611792-29612062	GM12878	blood:	n/a	n/a
12	BATF	chr22:29598610-29599251	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:29604981-29605256	GM12878	blood:	n/a	chr22:29605192-29605205
14	BCL11A	chr22:29598685-29599342	GM12878	blood:	n/a	chr22:29599010-29599023
15	BCL11A	chr22:29598759-29599229	GM12878	blood:	n/a	chr22:29599010-29599023
16	BCL3	chr22:29598723-29599254	GM12878	blood:	n/a	chr22:29599010-29599023
17	BCL3	chr22:29607384-29607821	GM12878	blood:	n/a	n/a
18	BCL3	chr22:29607350-29607787	GM12878	blood:	n/a	n/a
19	BCL3	chr22:29598254-29599363	GM12878	blood:	n/a	chr22:29599010-29599023
20	BCLAF1	chr22:29598254-29599470	GM12878	blood:	n/a	chr22:29599010-29599023
21	BCLAF1	chr22:29598192-29599296	GM12878	blood:	n/a	chr22:29599010-29599023
22	BHLHE40	chr22:29597979-29598898	K562	blood:	n/a	n/a
23	BHLHE40	chr22:29600224-29600481	GM12878	blood:	n/a	n/a
24	BHLHE40	chr22:29617036-29617131	HepG2	liver:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
25	BHLHE40	chr22:29601604-29602148	GM12878	blood:	n/a	chr22:29601941-29601957 chr22:29601938-29601954
26	BHLHE40	chr22:29616972-29617209	K562	blood:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
27	BHLHE40	chr22:29598272-29599266	GM12878	blood:	n/a	n/a
28	BHLHE40	chr22:29616987-29617222	GM12878	blood:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
29	BHLHE40	chr22:29591520-29591940	K562	blood:	n/a	n/a
30	BHLHE40	chr22:29602067-29602341	K562	blood:	n/a	n/a
31	BHLHE40	chr22:29588501-29588850	K562	blood:	n/a	n/a
32	BHLHE40	chr22:29601418-29601614	K562	blood:	n/a	n/a
33	BRCA1	chr22:29598487-29599112	GM12878	blood:	n/a	n/a
34	CBX3	chr22:29591551-29591851	K562	blood:	n/a	n/a
35	CBX3	chr22:29591463-29591951	K562	blood:	n/a	n/a
36	CBX3	chr22:29601251-29601604	K562	blood:	n/a	n/a
37	CBX3	chr22:29591078-29591436	K562	blood:	n/a	n/a
38	CCNT2	chr22:29598114-29598585	K562	blood:	n/a	n/a
39	CCNT2	chr22:29601582-29602429	K562	blood:	n/a	chr22:29601689-29601698 chr22:29601818-29601827
40	CCNT2	chr22:29598854-29599111	K562	blood:	n/a	n/a
41	CCNT2	chr22:29591475-29592017	K562	blood:	n/a	chr22:29591969-29591978
42	CCNT2	chr22:29593102-29593334	K562	blood:	n/a	n/a
43	CEBPB	chr22:29593054-29593706	K562	blood:	n/a	n/a
44	CEBPB	chr22:29593027-29593445	HCT-116	colon:	n/a	n/a
45	CEBPB	chr22:29598412-29599415	GM12878	blood:	n/a	n/a
46	CEBPB	chr22:29613294-29613677	HepG2	liver:	n/a	chr22:29613465-29613476
47	CEBPB	chr22:29598894-29599202	GM12878	blood:	n/a	n/a
48	CEBPB	chr22:29591526-29591814	K562	blood:	n/a	n/a
49	CEBPB	chr22:29613260-29613670	HepG2	liver:	n/a	chr22:29613465-29613476
50	CEBPB	chr22:29593086-29593310	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29601619-29601669	HCT-116	colon:	n/a
2	chr22:29601619-29601669	HCT-116	colon:	n/a
3	chr22:29601862-29601912	HCF	heart:	n/a
4	chr22:29601559-29601609	Jurkat	blood:	n/a
5	chr22:29602183-29602233	AG10803	skin:	n/a
6	chr22:29601763-29601813	AG10803	skin:	n/a
7	chr22:29601862-29601912	ovcar-3	ovarian:	n/a
8	chr22:29602004-29602054	ovcar-3	ovarian:	n/a
9	chr22:29601862-29601912	Caco-2	colon:	n/a
10	chr22:29598916-29598966	GM12891	blood:	n/a
11	chr22:29601559-29601609	SK-N-MC	brain:	n/a
12	chr22:29598916-29598966	NHBE	bronchial:	n/a
13	chr22:29605147-29605197	HRCEpiC	kidney:	n/a
14	chr22:29600657-29600707	MCF-7	breast:	n/a
15	chr22:29601862-29601912	NB4	blood:	n/a
16	chr22:29602004-29602054	K562	blood:	n/a
17	chr22:29598916-29598966	SK-N-MC	brain:	n/a
18	chr22:29602004-29602054	Caco-2	colon:	n/a
19	chr22:29603194-29603244	HAEpiC	amniotic membrane:	n/a
20	chr22:29600657-29600707	ProgFib	skin:	n/a
21	chr22:29601619-29601669	HPAEpiC	pulmonary alveolar:	n/a
22	chr22:29601862-29601912	AG04449	skin:	fetal
23	chr22:29600139-29600189	HRCEpiC	kidney:	n/a
24	chr22:29601860-29601910	CMK	blood:	n/a
25	chr22:29605147-29605197	SK-N-SH_RA	brain:	n/a
26	chr22:29601763-29601813	AoSMC	blood vessel:	n/a
27	chr22:29602183-29602233	SKMC	muscle:	n/a
28	chr22:29601559-29601609	PrEC	prostate:	n/a
29	chr22:29601619-29601669	RPTEC	kidney:	n/a
30	chr22:29605147-29605197	NB4	blood:	n/a
31	chr22:29600657-29600707	SK-N-MC	brain:	n/a
32	chr22:29598916-29598966	AG09319	gingival:	n/a
33	chr22:29601763-29601813	HAEpiC	amniotic membrane:	n/a
34	chr22:29600139-29600189	SK-N-SH_RA	brain:	n/a
35	chr22:29600657-29600707	HAEpiC	amniotic membrane:	n/a
36	chr22:29600139-29600189	T-47D	breast:	n/a
37	chr22:29601772-29601822	Jurkat	blood:	n/a
38	chr22:29600657-29600707	NHDF-neo	bronchial:	n/a
39	chr22:29601772-29601822	ProgFib	skin:	n/a
40	chr22:29600139-29600189	HAEpiC	amniotic membrane:	n/a
41	chr22:29598916-29598966	NHDF-neo	bronchial:	n/a
42	chr22:29600139-29600189	HCPEpiC	choroid plexus:	n/a
43	chr22:29601619-29601669	NHBE	bronchial:	n/a
44	chr22:29601862-29601912	NH-A	brain:	n/a
45	chr22:29601763-29601813	K562	blood:	n/a
46	chr22:29601862-29601912	HUVEC	blood vessel:	n/a
47	chr22:29601763-29601813	IMR90	lung:	fetal
48	chr22:29601860-29601910	HIPEpiC	eye:	n/a
49	chr22:29600139-29600189	HCT-116	colon:	n/a
50	chr22:29600139-29600189	HL-60	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29598698..29599406-chr22:29641204..29641781,2	K562	blood:
2	chr22:29612167..29614111-chr22:29627917..29629464,2	K562	blood:
3	chr22:29612019..29613931-chr22:29615202..29617842,2	MCF-7	breast:
4	chr22:29616773..29618442-chr22:29619234..29622066,2	MCF-7	breast:
5	chr22:29601072..29604199-chr22:29606005..29610482,4	MCF-7	breast:
6	chr22:29588962..29590714-chr22:29595745..29598495,3	K562	blood:
7	chr22:29601210..29603979-chr22:29627327..29629637,2	K562	blood:
8	chr22:29598167..29600634-chr22:29663372..29666044,2	K562	blood:
9	chr22:29612019..29613931-chr22:29615202..29617842,2	MCF-7	breast:
10	chr22:29616106..29618160-chr22:29628448..29630302,2	K562	blood:
11	chr22:29619482..29621531-chr22:29625031..29626896,2	K562	blood:
12	chr22:29618425..29620618-chr22:29628418..29631413,2	K562	blood:
13	chr22:29602636..29604550-chr22:29611942..29613555,2	K562	blood:
14	chr22:29598605..29599258-chr22:29640938..29642145,5	MCF-7	breast:
15	chr22:29612161..29619581-chr22:29619796..29623989,9	K562	blood:
16	chr22:29617283..29619466-chr22:29651521..29653548,2	K562	blood:
17	chr22:29601873..29603950-chr22:29609240..29612185,2	MCF-7	breast:
18	chr22:29585002..29586598-chr22:29591527..29594079,2	MCF-7	breast:
19	chr22:29605515..29607665-chr22:29648338..29651149,2	K562	blood:
20	chr22:29601873..29603950-chr22:29609240..29612185,2	MCF-7	breast:
21	chr22:29588962..29590714-chr22:29595745..29598495,3	K562	blood:
22	chr22:29585002..29586598-chr22:29591527..29594079,2	MCF-7	breast:
23	chr22:29581387..29582891-chr22:29590822..29592585,2	K562	blood:
24	chr22:29600453..29603035-chr22:29615819..29618230,2	K562	blood:
25	chr22:29289372..29291896-chr22:29597783..29600686,2	MCF-7	breast:
26	chr22:29616773..29618442-chr22:29619234..29622066,2	MCF-7	breast:
27	chr22:29617687..29619581-chr22:29621568..29623250,2	K562	blood:
28	chr22:29600704..29601509-chr22:29641190..29641939,2	MCF-7	breast:
29	chr22:29598263..29599277-chr22:29640793..29642655,17	MCF-7	breast:
30	chr22:29591219..29593786-chr22:29664964..29667623,2	K562	blood:
31	chr22:29609413..29611410-chr22:29651943..29654586,2	MCF-7	breast:
32	chr22:29619234..29621532-chr22:29627625..29630372,2	MCF-7	breast:
33	chr22:29601902..29603639-chr22:29605724..29608269,2	K562	blood:
34	chr22:29611701..29614819-chr22:29620518..29622673,3	K562	blood:
35	chr22:29579157..29580861-chr22:29584345..29586693,2	K562	blood:
36	chr22:29603086..29606057-chr22:29664265..29665857,2	MCF-7	breast:
37	chr22:29599772..29601516-chr22:29662820..29665325,2	K562	blood:
38	chr22:29611701..29614819-chr22:29620518..29622673,3	K562	blood:
39	chr22:29612161..29619581-chr22:29619796..29623989,9	K562	blood:
40	chr13:60970151..60970804-chr22:29601495..29602051,2	HCT-116	colon:
41	chr22:29609378..29611506-chr22:29620734..29622343,2	MCF-7	breast:
42	chr22:29601808..29604222-chr22:29612669..29614934,2	MCF-7	breast:
43	chr22:29602636..29604550-chr22:29611942..29613555,2	K562	blood:
44	chr22:29616331..29618039-chr22:29656036..29658500,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EWSR1-3	chr22:29620225-29620479	expReg_chr22_2008_+
2	lnc-EMID1-2	chr22:29589121-29589390	NONHSAT084679

No data

Variant related genes	Relation type
EMID1	TF binding region
RNU6-1219P	TF binding region
EMID1	CpG island
RNU6-1219P	CpG island
ENSG00000083544	chromatin interactions
ENSG00000186998	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000237015	chromatin interactions

Extended variants
information (count: 1335 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11704738	chr22:29586058-29586059	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs78187158	chr22:29586059-29586060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs571870543	chr22:29586066-29586067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544052313	chr22:29586131-29586132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117898123	chr22:29586132-29586133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577472524	chr22:29586140-29586141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568157463	chr22:29586160-29586161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs368897354	chr22:29586188-29586189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559990955	chr22:29586208-29586209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536703034	chr22:29586264-29586265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148917714	chr22:29586310-29586311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73397098	chr22:29586350-29586351	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs530879286	chr22:29586351-29586352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551965730	chr22:29586365-29586366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183777668	chr22:29586374-29586375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142243223	chr22:29586384-29586385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546616381	chr22:29586423-29586424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533592164	chr22:29586424-29586425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs114772642	chr22:29586430-29586431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374761083	chr22:29586447-29586448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568989671	chr22:29586449-29586450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs367822163	chr22:29586464-29586465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115800326	chr22:29586537-29586538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576565397	chr22:29586551-29586552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559198275	chr22:29586583-29586584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186948249	chr22:29586701-29586702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545470982	chr22:29586717-29586718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191735089	chr22:29586721-29586722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs151221940	chr22:29586753-29586754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183517710	chr22:29586810-29586811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6006053	chr22:29586824-29586825	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs369541816	chr22:29586831-29586832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4380342	chr22:29586832-29586833	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs111772635	chr22:29586846-29586847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564233699	chr22:29586849-29586850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528307579	chr22:29586867-29586868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111900618	chr22:29586881-29586882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568283507	chr22:29586909-29586910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371537333	chr22:29586910-29586911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144633933	chr22:29586912-29586913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs527579492	chr22:29586913-29586914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368220514	chr22:29586917-29586918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568823553	chr22:29586935-29586936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540669540	chr22:29586948-29586949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs71327339	chr22:29587012-29587013	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557925542	chr22:29587032-29587033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532678653	chr22:29587088-29587089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556965030	chr22:29587097-29587098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552410262	chr22:29587100-29587101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6006054	chr22:29587128-29587129	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD

Chromatin state (count:1133 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29572800-29591000	Weak transcription	Spleen	Spleen
2	chr22:29576400-29591000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr22:29576600-29590400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr22:29576600-29591200	Weak transcription	Fetal Intestine Small	intestine
5	chr22:29577600-29591200	Weak transcription	Dnd41	blood
6	chr22:29579200-29590600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr22:29580600-29591000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr22:29581200-29591400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr22:29581400-29586200	Weak transcription	Brain Cingulate Gyrus	brain
10	chr22:29581600-29598400	Weak transcription	Fetal Brain Female	brain
11	chr22:29583800-29588000	Enhancers	Fetal Brain Male	brain
12	chr22:29584200-29588600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr22:29584600-29591600	Weak transcription	Fetal Muscle Leg	muscle
14	chr22:29584800-29591600	Weak transcription	Brain Germinal Matrix	brain
15	chr22:29586200-29586400	Enhancers	Brain Cingulate Gyrus	brain
16	chr22:29588000-29598200	Weak transcription	Fetal Brain Male	brain
17	chr22:29588600-29588800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr22:29588600-29589000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr22:29588600-29589400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr22:29588600-29589400	Enhancers	K562	blood
21	chr22:29588800-29589200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:29589000-29591400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr22:29589200-29591200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:29589400-29591000	Weak transcription	K562	blood
25	chr22:29589400-29591400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr22:29589600-29597800	Weak transcription	Fetal Intestine Large	intestine
27	chr22:29590400-29590800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
28	chr22:29590600-29593200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr22:29590800-29591000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr22:29591000-29591600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr22:29591000-29591600	Enhancers	K562	blood
32	chr22:29591000-29591800	Enhancers	Spleen	Spleen
33	chr22:29591000-29592400	Enhancers	Primary hematopoietic stem cells	blood
34	chr22:29591000-29592600	Enhancers	Fetal Heart	heart
35	chr22:29591000-29592800	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr22:29591200-29591400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr22:29591200-29591400	Enhancers	Fetal Intestine Small	intestine
38	chr22:29591200-29592000	Enhancers	Right Ventricle	heart
39	chr22:29591200-29592200	Enhancers	Fetal Thymus	thymus
40	chr22:29591200-29592200	Genic enhancers	Dnd41	blood
41	chr22:29591200-29592400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr22:29591200-29592400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr22:29591200-29592400	Enhancers	Lung	lung
44	chr22:29591200-29592400	Bivalent Enhancer	HepG2	liver
45	chr22:29591200-29592800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr22:29591400-29591600	Genic enhancers	Fetal Intestine Small	intestine
47	chr22:29591400-29591800	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr22:29591400-29592000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr22:29591400-29592000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr22:29591400-29592000	Enhancers	Fetal Lung	lung

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