Variant report

Variant	nsv914978
Chromosome Location	chr22:31897795-31942770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:31926449-31927040	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:31940907-31941077	HepG2	liver:	n/a	n/a
3	ATF2	chr22:31932812-31933569	GM12878	blood:	n/a	n/a
4	ATF2	chr22:31934659-31935425	GM12878	blood:	n/a	n/a
5	ATF2	chr22:31932852-31933662	GM12878	blood:	n/a	n/a
6	ATF2	chr22:31934714-31935235	GM12878	blood:	n/a	n/a
7	BATF	chr22:31932926-31933388	GM12878	blood:	n/a	n/a
8	BATF	chr22:31916048-31916368	GM12878	blood:	n/a	n/a
9	BATF	chr22:31934780-31935139	GM12878	blood:	n/a	n/a
10	BATF	chr22:31940880-31941085	GM12878	blood:	n/a	n/a
11	BATF	chr22:31932933-31933569	GM12878	blood:	n/a	n/a
12	BATF	chr22:31940080-31940317	GM12878	blood:	n/a	chr22:31940238-31940249
13	BATF	chr22:31916079-31916329	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:31934808-31935153	GM12878	blood:	n/a	n/a
15	BCL11A	chr22:31932986-31933351	GM12878	blood:	n/a	n/a
16	BCL3	chr22:31932953-31933350	GM12878	blood:	n/a	n/a
17	BCL3	chr22:31928591-31928965	GM12878	blood:	n/a	n/a
18	BCLAF1	chr22:31932868-31933326	GM12878	blood:	n/a	n/a
19	BCLAF1	chr22:31934354-31935291	GM12878	blood:	n/a	n/a
20	BCLAF1	chr22:31932863-31933451	GM12878	blood:	n/a	n/a
21	BCLAF1	chr22:31934748-31935242	GM12878	blood:	n/a	n/a
22	BHLHE40	chr22:31934815-31935180	GM12878	blood:	n/a	n/a
23	CEBPB	chr22:31921507-31921779	IMR90	lung:	n/a	chr22:31921653-31921664
24	CEBPB	chr22:31921493-31921769	HepG2	liver:	n/a	chr22:31921653-31921664
25	CEBPB	chr22:31921448-31921784	MCF-7	breast:	n/a	chr22:31921653-31921664
26	CEBPB	chr22:31900299-31900814	IMR90	lung:	n/a	n/a
27	CEBPB	chr22:31900440-31900533	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr22:31938138-31938359	IMR90	lung:	n/a	n/a
29	CEBPB	chr22:31921516-31921764	A549	lung:	n/a	chr22:31921653-31921664
30	CEBPB	chr22:31934488-31935305	GM12878	blood:	n/a	n/a
31	CEBPB	chr22:31926498-31926727	HepG2	liver:	n/a	n/a
32	CEBPB	chr22:31926493-31927001	IMR90	lung:	n/a	n/a
33	CEBPB	chr22:31921591-31921766	H1-hESC	embryonic stem cell:	n/a	chr22:31921653-31921664
34	CEBPB	chr22:31938168-31938250	HepG2	liver:	n/a	n/a
35	CEBPB	chr22:31921636-31921697	K562	blood:	n/a	chr22:31921653-31921664
36	CHD2	chr22:31934730-31935160	GM12878	blood:	n/a	n/a
37	CREB1	chr22:31934640-31935386	GM12878	blood:	n/a	n/a
38	CREB1	chr22:31934655-31935251	GM12878	blood:	n/a	n/a
39	CREB1	chr22:31932767-31933714	GM12878	blood:	n/a	n/a
40	CREB1	chr22:31932905-31933605	GM12878	blood:	n/a	n/a
41	CTCF	chr22:31940623-31940681	GM19239	blood:	n/a	n/a
42	CTCF	chr22:31929328-31929418	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr22:31898029-31898099	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr22:31928340-31928490	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr22:31906423-31906530	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr22:31928260-31928410	AG04449	skin:	n/a	n/a
47	CUX1	chr22:31924685-31924782	GM12878	blood:	n/a	n/a
48	E2F4	chr22:31926749-31927028	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr22:31934822-31935103	GM12878	blood:	n/a	n/a
50	EBF1	chr22:31932934-31933419	GM12878	blood:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	22:31936958-31958600..22:32228866-32235273	K562	blood:
2	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
3	chr22:31895644..31897585-chr22:31899488..31902230,2	K562	blood:
4	chr22:31915170..31916943-chr22:31918334..31921689,3	K562	blood:
5	22:31936958-31958600..22:32740683-32750950	Hela-S3	cervix:
6	chr22:31892881..31894794-chr22:31897314..31900016,2	K562	blood:
7	chr22:31884404..31886896-chr22:31898271..31902090,3	MCF-7	breast:
8	chr22:31892596..31895248-chr22:31897166..31900535,3	MCF-7	breast:
9	22:31930706-31935473..22:32012966-32043914	GM12878	blood:
10	22:31936958-31958600..22:32342898-32343477	GM12878	blood:
11	22:31936958-31958600..22:32264718-32278135	Hela-S3	cervix:
12	chr22:31928865..31930656-chr22:31938813..31940821,2	MCF-7	breast:
13	22:31936958-31958600..22:32053085-32061138	Hela-S3	cervix:
14	22:31936958-31958600..22:32188129-32210582	K562	blood:
15	22:31936958-31958600..22:32477762-32487457	Hela-S3	cervix:
16	chr22:31926551..31928354-chr22:31935476..31937024,2	K562	blood:
17	22:31936958-31958600..22:31978142-31983723	K562	blood:
18	22:31936958-31958600..22:32170492-32188129	GM12878	blood:
19	22:31936958-31958600..22:33262063-33266567	K562	blood:
20	chr22:31915170..31916943-chr22:31918334..31921689,3	K562	blood:
21	chr22:31907252..31908998-chr22:32028816..32030585,2	MCF-7	breast:
22	chr22:31901562..31903154-chr22:32024706..32027058,2	MCF-7	breast:
23	22:31936958-31958600..22:32750950-32761732	Hela-S3	cervix:
24	chr22:31883080..31888273-chr22:31897152..31901136,10	MCF-7	breast:
25	22:31864703-31891033..22:31936958-31958600	GM12878	blood:
26	22:31936958-31958600..22:32162110-32166713	GM12878	blood:
27	22:31936958-31958600..22:32338420-32342898	K562	blood:
28	22:31936007-31936880..22:32338420-32342898	K562	blood:
29	chr22:31926551..31928354-chr22:31935476..31937024,2	K562	blood:
30	22:31936958-31958600..22:32292186-32294405	K562	blood:
31	22:31936958-31958600..22:32868055-32872511	K562	blood:
32	chr22:31928865..31930656-chr22:31938813..31940821,2	MCF-7	breast:
33	chr22:31890839..31893648-chr22:31927423..31929799,2	MCF-7	breast:
34	22:31936958-31958600..22:32860159-32865649	K562	blood:
35	chr22:31892433..31894421-chr22:31898516..31901632,3	K562	blood:
36	22:31836635-31847259..22:31936958-31958600	GM12878	blood:
37	22:31936958-31958600..22:32012966-32043914	GM12878	blood:
38	22:31864703-31891033..22:31930706-31935473	GM12878	blood:
39	22:31936958-31958600..22:32764253-32784733	K562	blood:
40	22:31936958-31958600..22:32594665-32606395	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084895
2	lnc-SFI1-2	chr22:31917221-31917306	NONHSAT084896
3	lnc-SFI1-2	chr22:31924676-31925053	NONHSAT084895
4	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084896
5	lnc-EIF4ENIF1-4	chr22:31917185-31917578	NONHSAT084897
6	lnc-EIF4ENIF1-5	chr22:31934338-31934575	NONHSAT084898
7	lnc-SFI1-2	chr22:31924676-31924852	NONHSAT084896

No data

Variant related genes	Relation type
ENSG00000229169	TF binding region
H2AFZP6	TF binding region
SFI1	TF binding region
ENSG00000198089	chromatin interactions
ENSG00000128253	chromatin interactions
ENSG00000128245	chromatin interactions
ENSG00000271093	chromatin interactions
ENSG00000100150	chromatin interactions
ENSG00000184459	chromatin interactions
ENSG00000242082	chromatin interactions
ENSG00000185666	chromatin interactions
ENSG00000241954	chromatin interactions
ENSG00000128254	chromatin interactions
ENSG00000232218	chromatin interactions
ENSG00000128276	chromatin interactions
ENSG00000205853	chromatin interactions
ENSG00000254127	chromatin interactions
ENSG00000100170	chromatin interactions
ENSG00000184708	chromatin interactions
ENSG00000199248	chromatin interactions
ENSG00000252909	chromatin interactions
ENSG00000230736	chromatin interactions
ENSG00000100225	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000243519	chromatin interactions

Extended variants
information (count: 1682 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1682 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9609304	chr22:31897795-31897796	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536885990	chr22:31897862-31897863	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192783511	chr22:31897866-31897867	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201188385	chr22:31897882-31897883	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs184225213	chr22:31897891-31897892	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs190718314	chr22:31897909-31897910	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555487746	chr22:31897922-31897923	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557757938	chr22:31897926-31897927	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572450954	chr22:31897962-31897963	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554728397	chr22:31897986-31897987	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs199605169	chr22:31897988-31897989	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577594230	chr22:31897998-31897999	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs374776777	chr22:31898063-31898064	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs540121132	chr22:31898113-31898114	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs560056377	chr22:31898152-31898153	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs573496452	chr22:31898178-31898179	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs542416085	chr22:31898205-31898206	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562799927	chr22:31898216-31898217	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs117819331	chr22:31898257-31898258	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147283225	chr22:31898268-31898269	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565258847	chr22:31898280-31898281	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs527729830	chr22:31898324-31898325	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs548108862	chr22:31898339-31898340	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75912920	chr22:31898363-31898364	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs567965270	chr22:31898366-31898367	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs74331731	chr22:31898377-31898378	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79419186	chr22:31898378-31898379	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs193030433	chr22:31898422-31898423	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550366030	chr22:31898452-31898453	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs369055006	chr22:31898462-31898463	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537925445	chr22:31898545-31898546	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs184363181	chr22:31898548-31898549	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577208763	chr22:31898576-31898577	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs188745293	chr22:31898635-31898636	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs181540802	chr22:31898640-31898641	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs372828299	chr22:31898645-31898646	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs573605783	chr22:31898655-31898656	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542377427	chr22:31898667-31898668	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs116322285	chr22:31898701-31898702	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558589861	chr22:31898732-31898733	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs57125303	chr22:31898750-31898751	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs564339361	chr22:31898783-31898784	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144850335	chr22:31898791-31898792	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185619398	chr22:31898878-31898879	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs547824027	chr22:31898903-31898904	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs578175158	chr22:31898989-31898990	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530439630	chr22:31898990-31898991	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs76874774	chr22:31899040-31899041	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs58386828	chr22:31899059-31899060	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs74586484	chr22:31899062-31899063	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 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
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
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
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
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:921 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31893000-31905200	Weak transcription	Aorta	Aorta
2	chr22:31893200-31903600	Weak transcription	Left Ventricle	heart
3	chr22:31893200-31912200	Weak transcription	Small Intestine	intestine
4	chr22:31893200-31934800	Weak transcription	Ovary	ovary
5	chr22:31893400-31900000	Weak transcription	HSMM	muscle
6	chr22:31893400-31905200	Weak transcription	Fetal Intestine Large	intestine
7	chr22:31893400-31907200	Weak transcription	Fetal Intestine Small	intestine
8	chr22:31893400-31909000	Weak transcription	Liver	Liver
9	chr22:31893400-31920400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr22:31893400-31971200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr22:31893600-31899800	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr22:31893600-31900000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr22:31893600-31900000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr22:31893600-31900000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr22:31893600-31900000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr22:31893600-31900000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr22:31893600-31900000	Weak transcription	NHDF-Ad	bronchial
18	chr22:31893600-31904600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr22:31893600-31904600	Weak transcription	A549	lung
20	chr22:31893600-31904800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr22:31893600-31907000	Weak transcription	Lung	lung
22	chr22:31893600-31909000	Weak transcription	Fetal Brain Male	brain
23	chr22:31893600-31925600	Weak transcription	Gastric	stomach
24	chr22:31893600-31926200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr22:31893600-31928200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr22:31893600-31934800	Weak transcription	Pancreas	Pancrea
27	chr22:31893600-31946600	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr22:31893600-31970000	Weak transcription	Colonic Mucosa	Colon
29	chr22:31893800-31897800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr22:31893800-31897800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr22:31893800-31897800	Weak transcription	Spleen	Spleen
32	chr22:31893800-31899000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr22:31893800-31900600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr22:31893800-31904800	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr22:31893800-31907000	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr22:31893800-31907400	Weak transcription	Right Ventricle	heart
37	chr22:31893800-31913400	Weak transcription	Fetal Muscle Leg	muscle
38	chr22:31893800-31914600	Weak transcription	HepG2	liver
39	chr22:31893800-31921800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr22:31893800-31924600	Weak transcription	Adipose Nuclei	Adipose
41	chr22:31893800-31924600	Weak transcription	Duodenum Mucosa	Duodenum
42	chr22:31893800-31925200	Weak transcription	Brain Hippocampus Middle	brain
43	chr22:31893800-31925400	Weak transcription	Brain Angular Gyrus	brain
44	chr22:31893800-31925600	Weak transcription	Rectal Smooth Muscle	rectum
45	chr22:31893800-31926400	Weak transcription	Fetal Lung	lung
46	chr22:31893800-31927000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr22:31893800-31934800	Weak transcription	HMEC	breast
48	chr22:31893800-31945600	Weak transcription	Brain Anterior Caudate	brain
49	chr22:31894000-31897800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr22:31894000-31900200	Weak transcription	NHEK	skin

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