Variant report

Variant	rs34988612
Chromosome Location	chr20:29611823-29611824
allele	A/G
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	POLR2A	chr20:29610805-29612449	K562	blood:	n/a	n/a
2	TAF1	chr20:29611464-29612400	SK-N-SH	brain:	n/a	n/a
3	CTCF	chr20:29611760-29611910	A549	lung:	n/a	n/a
4	CBX3	chr20:29610759-29612458	K562	blood:	n/a	n/a
5	POLR2A	chr20:29611546-29612132	HepG2	liver:	n/a	n/a
6	BHLHE40	chr20:29610925-29612439	K562	blood:	n/a	chr20:29611694-29611710 chr20:29611686-29611702
7	TAF1	chr20:29611741-29612415	ECC-1	luminal epithelium:	n/a	n/a
8	POLR2A	chr20:29611099-29612401	A549	lung:	n/a	n/a
9	GTF2B	chr20:29611609-29612188	K562	blood:	n/a	n/a
10	ELF1	chr20:29611351-29612187	HCT-116	colon:	n/a	n/a
11	ELF1	chr20:29611601-29612116	A549	lung:	n/a	n/a
12	POU2F2	chr20:29611598-29611829	GM12878	blood:	n/a	n/a
13	POLR2A	chr20:29611492-29612362	NB4	blood:	n/a	n/a
14	SPI1	chr20:29611563-29612046	K562	blood:	n/a	n/a
15	PAX5	chr20:29611503-29612446	GM12878	blood:	n/a	n/a
16	JUND	chr20:29611117-29612572	K562	blood:	n/a	chr20:29611833-29611842 chr20:29611838-29611847 chr20:29611832-29611841 chr20:29611836-29611845 chr20:29612436-29612445 chr20:29611837-29611846 chr20:29611839-29611848 chr20:29611835-29611844
17	POLR2A	chr20:29610824-29612470	PANC-1	pancreas:	n/a	n/a
18	POLR2A	chr20:29611431-29612428	K562	blood:	n/a	n/a
19	MAX	chr20:29611009-29612352	K562	blood:	n/a	chr20:29611840-29611850
20	CEBPB	chr20:29611623-29611943	HepG2	liver:	n/a	n/a
21	RAD21	chr20:29611521-29611982	K562	blood:	n/a	chr20:29611752-29611771
22	SIX5	chr20:29611589-29612044	A549	lung:	n/a	n/a
23	CTCF	chr20:29611625-29611843	Spleen_OC	spleen:	n/a	chr20:29611752-29611768 chr20:29611751-29611769 chr20:29611754-29611767
24	USF1	chr20:29611537-29611841	HepG2	liver:	n/a	chr20:29611694-29611710 chr20:29611686-29611702
25	POLR2A	chr20:29609499-29613259	GM12892	blood:	n/a	n/a
26	CTCF	chr20:29611541-29611837	SK-N-SH_RA	brain:	n/a	chr20:29611752-29611768 chr20:29611751-29611769 chr20:29611754-29611767
27	POLR2A	chr20:29611493-29612385	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr20:29611611-29611857	Gliobla	brain:	n/a	chr20:29611752-29611768 chr20:29611751-29611769 chr20:29611754-29611767
29	ZBTB33	chr20:29609453-29612585	K562	blood:	n/a	n/a
30	MAZ	chr20:29610923-29612179	HepG2	liver:	n/a	chr20:29611840-29611850
31	MAX	chr20:29611249-29612130	HCT-116	colon:	n/a	chr20:29611840-29611850
32	JUND	chr20:29611086-29612126	A549	lung:	n/a	chr20:29611833-29611842 chr20:29611838-29611847 chr20:29611832-29611841 chr20:29611836-29611845 chr20:29611837-29611846 chr20:29611839-29611848 chr20:29611835-29611844
33	NR2F2	chr20:29610867-29612670	K562	blood:	n/a	n/a
34	POLR2A	chr20:29611165-29612370	K562	blood:	n/a	n/a
35	IRF1	chr20:29611600-29612021	K562	blood:	n/a	chr20:29611827-29611841
36	CTCF	chr20:29611680-29611830	HUVEC	blood vessel:	n/a	chr20:29611752-29611768 chr20:29611751-29611769 chr20:29611754-29611767
37	CEBPD	chr20:29611537-29612051	HepG2	liver:	n/a	n/a
38	MXI1	chr20:29611069-29612188	K562	blood:	n/a	n/a
39	POLR2A	chr20:29611548-29612435	SK-N-SH	brain:	n/a	n/a
40	TAF1	chr20:29611075-29612429	GM12891	blood:	n/a	n/a
41	CEBPB	chr20:29611198-29611862	K562	blood:	n/a	n/a
42	ETS1	chr20:29611385-29612412	K562	blood:	n/a	chr20:29611836-29611847 chr20:29611831-29611842 chr20:29611837-29611848 chr20:29611839-29611850 chr20:29611488-29611501 chr20:29611834-29611845
43	POLR2A	chr20:29611190-29612432	K562	blood:	n/a	n/a
44	CEBPD	chr20:29611432-29612481	K562	blood:	n/a	n/a
45	POLR2A	chr20:29611177-29612365	Gliobla	brain:	n/a	n/a
46	REST	chr20:29611511-29612430	SK-N-SH	brain:	n/a	chr20:29611684-29611697 chr20:29611692-29611706 chr20:29611580-29611593
47	SP2	chr20:29611820-29611982	K562	blood:	n/a	n/a
48	ZBTB33	chr20:29611561-29611931	HepG2	liver:	n/a	n/a
49	SIN3AK20	chr20:29611465-29612435	K562	blood:	n/a	n/a
50	ZBTB33	chr20:29611601-29612033	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:29611796-29611846	PrEC	prostate:	n/a
2	chr20:29611785-29611835	U87	brain:	n/a
3	chr20:29611810-29611860	AoSMC	blood vessel:	n/a
4	chr20:29611785-29611835	MCF10A-Er-Src	breast:	n/a
5	chr20:29611796-29611846	K562	blood:	n/a
6	chr20:29611785-29611835	SAEC	small airway:	n/a
7	chr20:29611785-29611835	SK-N-SH	brain:	n/a
8	chr20:29611796-29611846	HAEpiC	amniotic membrane:	n/a
9	chr20:29611810-29611860	AG09309	skin:	n/a
10	chr20:29611810-29611860	HMEC	breast:	n/a
11	chr20:29611785-29611835	HEEpiC	esophagus:	n/a
12	chr20:29611810-29611860	NHDF-neo	bronchial:	n/a
13	chr20:29611785-29611835	AG09309	skin:	n/a
14	chr20:29611810-29611860	SK-N-SH_RA	brain:	n/a
15	chr20:29611796-29611846	NH-A	brain:	n/a
16	chr20:29611810-29611860	NH-A	brain:	n/a
17	chr20:29611785-29611835	IMR90	lung:	fetal
18	chr20:29611785-29611835	SK-N-MC	brain:	n/a
19	chr20:29611796-29611846	Hepatocyte	liver:	n/a
20	chr20:29611785-29611835	PFSK-1	brain:	n/a
21	chr20:29611796-29611846	GM06990	blood:	n/a
22	chr20:29611785-29611835	HepG2	liver:	n/a
23	chr20:29611796-29611846	Hela-S3	cervix:	n/a
24	chr20:29611796-29611846	MCF-7	breast:	n/a
25	chr20:29611785-29611835	AG04449	skin:	fetal
26	chr20:29611785-29611835	SKMC	muscle:	n/a
27	chr20:29611796-29611846	HRE	kidney:	n/a
28	chr20:29611796-29611846	SAEC	small airway:	n/a
29	chr20:29611796-29611846	NHDF-neo	bronchial:	n/a
30	chr20:29611810-29611860	Hepatocyte	liver:	n/a
31	chr20:29611810-29611860	GM19239	blood:	n/a
32	chr20:29611796-29611846	AG09319	gingival:	n/a
33	chr20:29611796-29611846	SK-N-MC	brain:	n/a
34	chr20:29611785-29611835	HUVEC	blood vessel:	n/a
35	chr20:29611796-29611846	AG09309	skin:	n/a
36	chr20:29611785-29611835	ECC-1	luminal epithelium:	n/a
37	chr20:29611810-29611860	HEEpiC	esophagus:	n/a
38	chr20:29611810-29611860	MCF-7	breast:	n/a
39	chr20:29611785-29611835	HEK293	kidney:	embryo
40	chr20:29611785-29611835	HL-60	blood:	n/a
41	chr20:29611785-29611835	AG04450	lung:	fetal
42	chr20:29611810-29611860	AG04450	lung:	fetal
43	chr20:29611810-29611860	T-47D	breast:	n/a
44	chr20:29611810-29611860	HNPCEpiC	eye:	n/a
45	chr20:29611796-29611846	HCF	heart:	n/a
46	chr20:29611796-29611846	HepG2	liver:	n/a
47	chr20:29611810-29611860	RPTEC	kidney:	n/a
48	chr20:29611796-29611846	PANC-1	pancreas:	n/a
49	chr20:29611785-29611835	LNCaP	prostate:	n/a
50	chr20:29611785-29611835	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:29610673..29612888-chr4:190860203..190862511,3	MCF-7	breast:
2	chr20:29610649..29612158-chr9:68453830..68455817,2	K562	blood:
3	chr20:29611632..29612497-chr4:190861809..190862721,3	MCF-7	breast:
4	chr20:29609593..29613129-chr4:190859723..190863221,5	K562	blood:
5	chr20:29611128..29612321-chr4:190861463..190862739,6	MCF-7	breast:
6	chr20:29611070..29612139-chr9:68455176..68456091,3	K562	blood:
7	chr20:29611427..29612170-chr9:68454810..68455955,3	MCF-7	breast:
8	chr20:29611333..29614057-chr4:190860675..190863034,4	MCF-7	breast:
9	chr20:29611384..29612018-chr9:68455093..68455961,3	MCF-7	breast:
10	chr2:133109798..133110355-chr20:29611407..29612129,2	MCF-7	breast:
11	chr20:29610847..29613187-chr4:190860454..190862227,2	K562	blood:
12	chr20:29611467..29612118-chr9:68454964..68455886,2	MCF-7	breast:
13	chr20:29611333..29612723-chr4:190861521..190862825,5	HCT-116	colon:
14	chr20:29611329..29612191-chr9:68455368..68456077,2	MCF-7	breast:

Variant related genes	Relation type
FRG1B	TF binding region
FRG1B	CpG island
ENSG00000215548	Chromatin interaction
ENSG00000230992	Chromatin interaction
ENSG00000109536	Chromatin interaction
ENSG00000245685	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs6057191	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6057373	0.86[ASN][1000 genomes]
rs6057378	0.88[ASN][1000 genomes]
rs6057406	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6087167	0.93[ASN][1000 genomes]
rs6087264	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6118923	0.89[ASN][1000 genomes]
rs6119084	0.90[ASN][1000 genomes]
rs6119089	0.82[ASN][1000 genomes]
rs6119118	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6141218	0.91[ASN][1000 genomes]
rs8117830	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758518	chr20:29419570-29653908	Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv2758791	chr20:29419570-29653908	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv428028	chr20:29419570-29653908	Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv428376	chr20:29419570-29653908	Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv1062766	chr20:29420340-29635454	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv833950	chr20:29472154-29638425	Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1058387	chr20:29479828-29651199	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	esv2756736	chr20:29493193-29630695	ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv1067193	chr20:29525410-29651199	Enhancers ZNF genes & repeats Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	esv11674	chr20:29528011-29653880	Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv965870	chr20:29570138-29652376	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	esv3359503	chr20:29579591-29639989	ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	esv3336027	chr20:29579691-29639889	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
14	esv3337149	chr20:29579691-29639889	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	esv3343795	chr20:29579691-29639889	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	esv3380005	chr20:29579691-29639889	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	esv3441285	chr20:29579691-29639889	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	esv15335	chr20:29580700-29653880	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv585870	chr20:29603773-29648195	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:29609400-29614200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr20:29609600-29612400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:29610600-29614800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr20:29610600-29614800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
5	chr20:29610800-29612400	Active TSS	Fetal Heart	heart
6	chr20:29610800-29612400	ZNF genes & repeats	Spleen	Spleen
7	chr20:29610800-29612600	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
8	chr20:29610800-29612600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr20:29610800-29612600	ZNF genes & repeats	Gastric	stomach
10	chr20:29610800-29612800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
11	chr20:29610800-29612800	ZNF genes & repeats	Fetal Muscle Leg	muscle
12	chr20:29610800-29613000	ZNF genes & repeats	Fetal Stomach	stomach
13	chr20:29610800-29613400	ZNF genes & repeats	HMEC	breast
14	chr20:29610800-29613400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
15	chr20:29610800-29613600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
16	chr20:29610800-29613600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
17	chr20:29610800-29613600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
18	chr20:29610800-29613600	ZNF genes & repeats	Fetal Brain Male	brain
19	chr20:29610800-29614800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr20:29610800-29614800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
21	chr20:29611000-29612400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
22	chr20:29611000-29612400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr20:29611000-29612400	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr20:29611000-29612400	ZNF genes & repeats	Primary B cells from peripheral blood	blood
25	chr20:29611000-29612400	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
26	chr20:29611000-29612400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
27	chr20:29611000-29612400	ZNF genes & repeats	Liver	Liver
28	chr20:29611000-29612400	ZNF genes & repeats	Brain Anterior Caudate	brain
29	chr20:29611000-29612400	ZNF genes & repeats	Colonic Mucosa	Colon
30	chr20:29611000-29612400	ZNF genes & repeats	Thymus	Thymus
31	chr20:29611000-29612400	ZNF genes & repeats	HSMMtube	muscle
32	chr20:29611000-29612400	ZNF genes & repeats	NHDF-Ad	bronchial
33	chr20:29611000-29612600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr20:29611000-29612600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr20:29611000-29612600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr20:29611000-29612600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr20:29611000-29612600	Active TSS	Primary T cells from cord blood	blood
38	chr20:29611000-29612600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr20:29611000-29612600	ZNF genes & repeats	Primary T helper 17 cells PMA-I stimulated	--
40	chr20:29611000-29612600	ZNF genes & repeats	Aorta	Aorta
41	chr20:29611000-29612600	ZNF genes & repeats	Esophagus	oesophagus
42	chr20:29611000-29612600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
43	chr20:29611000-29612800	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr20:29611000-29612800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
45	chr20:29611000-29612800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr20:29611000-29613000	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr20:29611000-29613000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr20:29611000-29613000	ZNF genes & repeats	Fetal Brain Female	brain
49	chr20:29611000-29613000	ZNF genes & repeats	Hela-S3	cervix
50	chr20:29611000-29613200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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