Variant report

Variant	nsv585730
Chromosome Location	chr20:23809681-23862844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:244)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23860701-23861025	HepG2	liver:	n/a	n/a
2	BACH1	chr20:23832673-23832794	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr20:23860610-23860881	HepG2	liver:	n/a	n/a
4	CEBPB	chr20:23828408-23828598	A549	lung:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
5	CEBPB	chr20:23860682-23861020	HepG2	liver:	n/a	chr20:23860869-23860880
6	CEBPB	chr20:23847533-23847686	A549	lung:	n/a	n/a
7	CEBPB	chr20:23828412-23828599	HepG2	liver:	n/a	chr20:23828517-23828526 chr20:23828517-23828528 chr20:23828515-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828517-23828526 chr20:23828515-23828528
8	CEBPB	chr20:23847524-23847664	HepG2	liver:	n/a	n/a
9	CEBPB	chr20:23848981-23849346	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr20:23852909-23852982	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr20:23860687-23860957	HepG2	liver:	n/a	n/a
12	CTCF	chr20:23823743-23823810	Fibrobl	skin:	n/a	n/a
13	CTCF	chr20:23828860-23828892	Fibrobl	skin:	n/a	n/a
14	CTCF	chr20:23826220-23826370	HEK293	kidney:	n/a	n/a
15	CTCF	chr20:23826230-23826361	HepG2	liver:	n/a	n/a
16	CTCF	chr20:23826266-23826336	K562	blood:	n/a	n/a
17	CTCF	chr20:23856560-23856710	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr20:23837515-23837733	MCF-7	breast:	n/a	n/a
19	CTCF	chr20:23826175-23826396	Gliobla	brain:	n/a	n/a
20	CTCF	chr20:23858260-23858410	SAEC	small airway:	n/a	chr20:23858391-23858409
21	CTCF	chr20:23858300-23858450	Caco-2	colon:	n/a	chr20:23858391-23858409
22	CTCF	chr20:23858520-23858670	GM12873	blood:	n/a	n/a
23	CTCF	chr20:23832056-23832136	GM13976	blood:	n/a	n/a
24	CTCF	chr20:23858320-23858470	HEK293	kidney:	n/a	chr20:23858391-23858409
25	CTCF	chr20:23858400-23858550	GM12869	blood:	n/a	n/a
26	CTCF	chr20:23826180-23826330	AG09309	skin:	n/a	n/a
27	CTCF	chr20:23856558-23856596	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr20:23821960-23822110	Caco-2	colon:	n/a	n/a
29	CTCF	chr20:23826207-23826394	MCF-7	breast:	n/a	n/a
30	CTCF	chr20:23826200-23826350	HCT-116	colon:	n/a	n/a
31	CTCF	chr20:23810371-23810443	GM13976	blood:	n/a	n/a
32	CTCF	chr20:23858400-23858550	HEK293	kidney:	n/a	n/a
33	CTCF	chr20:23858320-23858470	WERI-Rb-1	eye:	n/a	chr20:23858391-23858409
34	CTCF	chr20:23826180-23826330	A549	lung:	n/a	n/a
35	CTCF	chr20:23858280-23858430	GM12875	blood:	n/a	chr20:23858391-23858409
36	CTCF	chr20:23857980-23858130	HEK293	kidney:	n/a	n/a
37	CTCF	chr20:23816560-23816710	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr20:23826271-23826333	Medullo	brain:	n/a	n/a
39	CTCF	chr20:23825740-23825890	GM12867	blood:	n/a	n/a
40	CTCF	chr20:23837480-23837630	MCF-7	breast:	n/a	n/a
41	CTCF	chr20:23858040-23858190	GM12864	blood:	n/a	n/a
42	CTCF	chr20:23832700-23832850	GM12867	blood:	n/a	n/a
43	CTCF	chr20:23858240-23858390	GM12873	blood:	n/a	n/a
44	CTCF	chr20:23858420-23858570	RPTEC	kidney:	n/a	n/a
45	CTCF	chr20:23860040-23860190	HepG2	liver:	n/a	n/a
46	CTCF	chr20:23858260-23858410	WERI-Rb-1	eye:	n/a	chr20:23858391-23858409
47	CTCF	chr20:23858998-23859025	NHEK	skin:	n/a	n/a
48	CTCF	chr20:23823800-23823950	GM12874	blood:	n/a	n/a
49	CTCF	chr20:23826202-23826374	LNCaP	prostate:	n/a	n/a
50	CTCF	chr20:23837521-23837711	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23861239-23861289	AG10803	skin:	n/a
2	chr20:23860078-23860128	AG09309	skin:	n/a
3	chr20:23861239-23861289	PANC-1	pancreas:	n/a
4	chr20:23860242-23860292	SK-N-MC	brain:	n/a
5	chr20:23861280-23861330	NHBE	bronchial:	n/a
6	chr20:23860078-23860128	LNCaP	prostate:	n/a
7	chr20:23860078-23860128	HCM	heart:	n/a
8	chr20:23860078-23860128	BE2_C	brain:	n/a
9	chr20:23861239-23861289	BJ	skin:	n/a
10	chr20:23861239-23861289	IMR90	lung:	fetal
11	chr20:23860242-23860292	HPAEpiC	pulmonary alveolar:	n/a
12	chr20:23860078-23860128	NHDF-neo	bronchial:	n/a
13	chr20:23861239-23861289	AG09309	skin:	n/a
14	chr20:23861280-23861330	NH-A	brain:	n/a
15	chr20:23860242-23860292	ovcar-3	ovarian:	n/a
16	chr20:23861280-23861330	GM12878	blood:	n/a
17	chr20:23860078-23860128	AG09319	gingival:	n/a
18	chr20:23860078-23860128	AG04449	skin:	fetal
19	chr20:23861280-23861330	HEK293	kidney:	embryo
20	chr20:23861239-23861289	SAEC	small airway:	n/a
21	chr20:23860242-23860292	LNCaP	prostate:	n/a
22	chr20:23861239-23861289	Hela-S3	cervix:	n/a
23	chr20:23861239-23861289	K562	blood:	n/a
24	chr20:23860078-23860128	SKMC	muscle:	n/a
25	chr20:23861239-23861289	HCM	heart:	n/a
26	chr20:23861239-23861289	SKMC	muscle:	n/a
27	chr20:23861280-23861330	HepG2	liver:	n/a
28	chr20:23860242-23860292	NHDF-neo	bronchial:	n/a
29	chr20:23860242-23860292	NHBE	bronchial:	n/a
30	chr20:23860242-23860292	AG10803	skin:	n/a
31	chr20:23861239-23861289	AoSMC	blood vessel:	n/a
32	chr20:23860078-23860128	GM12892	blood:	n/a
33	chr20:23861239-23861289	HNPCEpiC	eye:	n/a
34	chr20:23861280-23861330	BJ	skin:	n/a
35	chr20:23860242-23860292	GM12891	blood:	n/a
36	chr20:23861239-23861289	AG09319	gingival:	n/a
37	chr20:23860242-23860292	AG04450	lung:	fetal
38	chr20:23861239-23861289	AG04450	lung:	fetal
39	chr20:23861239-23861289	SK-N-SH	brain:	n/a
40	chr20:23860078-23860128	GM12891	blood:	n/a
41	chr20:23860078-23860128	A549	lung:	n/a
42	chr20:23861239-23861289	RPTEC	kidney:	n/a
43	chr20:23861239-23861289	HRE	kidney:	n/a
44	chr20:23860078-23860128	HCT-116	colon:	n/a
45	chr20:23861239-23861289	ProgFib	skin:	n/a
46	chr20:23860078-23860128	CMK	blood:	n/a
47	chr20:23860078-23860128	SK-N-SH_RA	brain:	n/a
48	chr20:23861239-23861289	HEEpiC	esophagus:	n/a
49	chr20:23860078-23860128	Caco-2	colon:	n/a
50	chr20:23860078-23860128	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr20:23852729..23853709-chr9:66823512..66824018,2	MCF-7	breast:
2	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
3	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
4	chr20:23852729..23853709-chr9:66823514..66824015,2	MCF-7	breast:
5	chr11:62608849..62609515-chr20:23852729..23853229,2	MCF-7	breast:
6	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:
7	chr20:23852729..23853229-chr20:26319433..26319936,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-6	chr20:23854853-23855563	NONHSAT079087
2	lnc-CST8-6	chr20:23853000-23853122	NONHSAT079087

No data

Variant related genes	Relation type
CST5	TF binding region
CST2	TF binding region
CST5	CpG island
CST2	CpG island
ENSG00000133316	chromatin interactions

Extended variants
information (count: 2130 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2130 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6132672	chr20:23809681-23809682	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559423341	chr20:23809682-23809683	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs79833196	chr20:23809699-23809700	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs73094562	chr20:23809708-23809709	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs565093497	chr20:23809727-23809728	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs530685684	chr20:23809775-23809776	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs550739884	chr20:23809777-23809778	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs75449057	chr20:23809783-23809784	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs536284669	chr20:23809832-23809833	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs546551269	chr20:23809833-23809834	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs566316488	chr20:23809897-23809898	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs539334725	chr20:23809898-23809899	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs142555761	chr20:23809926-23809927	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs6138129	chr20:23809971-23809972	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs555418893	chr20:23809972-23809973	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs558943106	chr20:23809984-23809985	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs575435101	chr20:23810026-23810027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538047597	chr20:23810045-23810046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532243890	chr20:23810079-23810080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554684951	chr20:23810091-23810092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574576611	chr20:23810099-23810100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372907894	chr20:23810100-23810101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182114326	chr20:23810107-23810108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577132967	chr20:23810108-23810109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186648559	chr20:23810148-23810149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76311119	chr20:23810161-23810162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs530765297	chr20:23810172-23810173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550776667	chr20:23810173-23810174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560991513	chr20:23810177-23810178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550359178	chr20:23810182-23810183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546344204	chr20:23810183-23810184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566470981	chr20:23810184-23810185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191498772	chr20:23810189-23810190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6114321	chr20:23810199-23810200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552499349	chr20:23810206-23810207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569200198	chr20:23810209-23810210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577731622	chr20:23810212-23810213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538084301	chr20:23810219-23810220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs141443982	chr20:23810220-23810221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534318575	chr20:23810225-23810226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553935936	chr20:23810226-23810227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577174221	chr20:23810228-23810229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544963376	chr20:23810229-23810230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545866103	chr20:23810230-23810231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201776666	chr20:23810235-23810236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs7267330	chr20:23810238-23810239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575585641	chr20:23810239-23810240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs75511209	chr20:23810247-23810248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs367551079	chr20:23810250-23810251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561082309	chr20:23810268-23810269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23807400-23812200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr20:23807400-23812200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr20:23807400-23812400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr20:23807800-23811000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr20:23807800-23811000	Weak transcription	NHDF-Ad	bronchial
6	chr20:23807800-23812400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr20:23808000-23812200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr20:23808000-23812400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:23809000-23810000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr20:23809000-23812400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr20:23809600-23812200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr20:23811000-23813800	Enhancers	NHDF-Ad	bronchial
13	chr20:23811000-23814000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr20:23811200-23811400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr20:23811600-23812800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr20:23812200-23812800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr20:23812200-23813000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr20:23812200-23813200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr20:23812200-23813600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr20:23812200-23813600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr20:23812200-23814000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr20:23812400-23812600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr20:23812400-23813000	Enhancers	HUVEC	blood vessel
24	chr20:23812400-23813200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr20:23812400-23813200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr20:23812400-23813200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr20:23812400-23813200	Enhancers	Osteobl	bone
28	chr20:23812400-23814000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr20:23812400-23814600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:23812600-23813200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr20:23812800-23813800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr20:23813200-23813400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr20:23816200-23817400	Enhancers	Fetal Thymus	thymus
34	chr20:23816600-23816800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
35	chr20:23823600-23824000	Enhancers	Fetal Thymus	thymus
36	chr20:23832400-23832800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr20:23832400-23832800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr20:23832600-23833000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr20:23832600-23833000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr20:23832600-23833000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr20:23832800-23833000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:23832800-23838200	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr20:23832800-23838200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr20:23833000-23838000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr20:23833000-23846800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr20:23836400-23836800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr20:23836400-23837000	Enhancers	Fetal Thymus	thymus
48	chr20:23836400-23837200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr20:23836600-23836800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr20:23836800-23838000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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