Variant report

Variant	rs117867619
Chromosome Location	chr21:45148880-45148881
allele	G/T
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	chr21:45147277-45149094	GM12892	blood:	n/a	n/a
2	POLR2A	chr21:45148283-45149187	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr21:45146633-45148919	NB4	blood:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
4	ZNF263	chr21:45147349-45149233	HEK293-T-REx	kidney:	n/a	chr21:45148434-45148443 chr21:45148431-45148440 chr21:45148544-45148553
5	CTCFL	chr21:45148844-45149121	K562	blood:	n/a	chr21:45148970-45148979
6	CHD2	chr21:45148493-45148908	H1-hESC	embryonic stem cell:	n/a	n/a
7	ZMIZ1	chr21:45148227-45149155	K562	blood:	n/a	n/a
8	SP1	chr21:45148299-45148884	GM12878	blood:	n/a	chr21:45148608-45148619 chr21:45148417-45148426 chr21:45148429-45148443
9	GABPA	chr21:45148292-45148925	A549	lung:	n/a	chr21:45148529-45148538
10	JUND	chr21:45148226-45148922	H1-hESC	embryonic stem cell:	n/a	chr21:45148409-45148419 chr21:45148408-45148420 chr21:45148408-45148419 chr21:45148409-45148419 chr21:45148409-45148419 chr21:45148410-45148418 chr21:45148409-45148419
11	MXI1	chr21:45147556-45149627	SK-N-SH	brain:	n/a	n/a
12	TCF12	chr21:45148157-45148978	SK-N-SH	brain:	n/a	chr21:45148372-45148380
13	FOS	chr21:45148184-45148909	HUVEC	blood vessel:	n/a	chr21:45148409-45148419 chr21:45148408-45148420 chr21:45148409-45148419 chr21:45148409-45148419 chr21:45148408-45148419 chr21:45148410-45148418 chr21:45148409-45148419
14	EGR1	chr21:45148488-45148932	H1-hESC	embryonic stem cell:	n/a	chr21:45148559-45148573
15	MAX	chr21:45146914-45148973	HCT-116	colon:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
16	BCLAF1	chr21:45148295-45149208	GM12878	blood:	n/a	chr21:45148987-45148996 chr21:45148979-45148992 chr21:45148448-45148461 chr21:45148948-45148961
17	MAX	chr21:45148025-45149101	K562	blood:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
18	YY1	chr21:45148306-45148927	K562	blood:	n/a	n/a
19	POLR2A	chr21:45148217-45148987	GM12878	blood:	n/a	n/a
20	SPI1	chr21:45148423-45149035	HL-60	blood:	n/a	chr21:45148435-45148448
21	CHD2	chr21:45148254-45148990	GM12878	blood:	n/a	n/a
22	YY1	chr21:45148293-45149196	K562	blood:	n/a	chr21:45148979-45148993
23	TAF1	chr21:45148413-45148949	H1-hESC	embryonic stem cell:	n/a	n/a
24	RCOR1	chr21:45148137-45148882	K562	blood:	n/a	n/a
25	CEBPB	chr21:45148384-45149001	GM12878	blood:	n/a	n/a
26	GATA3	chr21:45147247-45148950	A549	lung:	n/a	chr21:45147517-45147525 chr21:45147247-45147257
27	RELA	chr21:45148270-45148952	GM19193	blood:	n/a	n/a
28	PML	chr21:45148053-45148964	K562	blood:	n/a	n/a
29	MYC	chr21:45148264-45148894	K562	blood:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
30	CTCF	chr21:45148860-45149010	HEK293	kidney:	n/a	n/a
31	RELA	chr21:45148254-45148907	GM10847	blood:	n/a	n/a
32	JUND	chr21:45148206-45148999	A549	lung:	n/a	chr21:45148409-45148419 chr21:45148408-45148420 chr21:45148408-45148419 chr21:45148409-45148419 chr21:45148409-45148419 chr21:45148953-45148962 chr21:45148410-45148418 chr21:45148409-45148419
33	MYC	chr21:45146778-45148912	NB4	blood:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
34	RAD21	chr21:45148862-45149086	K562	blood:	n/a	chr21:45148970-45148980
35	MAX	chr21:45147321-45149596	HepG2	liver:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45149136-45149146 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
36	POLR2A	chr21:45148112-45148959	K562	blood:	n/a	n/a
37	POLR2A	chr21:45148207-45148916	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr21:45148174-45149182	SK-N-SH	brain:	n/a	n/a
39	RELA	chr21:45148294-45148951	GM18951	blood:	n/a	n/a
40	ZBTB7A	chr21:45148597-45148907	HepG2	liver:	n/a	n/a
41	POLR2A	chr21:45148305-45148917	GM12891	blood:	n/a	n/a
42	POLR2A	chr21:45148175-45149050	HUVEC	blood vessel:	n/a	n/a
43	CCNT2	chr21:45147842-45149247	K562	blood:	n/a	chr21:45147962-45147971
44	REST	chr21:45148117-45149000	H1-neurons	neurons:	n/a	n/a
45	MAZ	chr21:45147913-45149088	HepG2	liver:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541
46	POLR2A	chr21:45147305-45148924	GM12878	blood:	n/a	n/a
47	POLR2A	chr21:45148141-45149230	GM12878	blood:	n/a	n/a
48	FOXM1	chr21:45148274-45148916	GM12878	blood:	n/a	n/a
49	POLR2A	chr21:45148203-45149303	H1-hESC	embryonic stem cell:	n/a	n/a
50	MYC	chr21:45148009-45148936	K562	blood:	n/a	chr21:45148531-45148540 chr21:45148566-45148581 chr21:45148190-45148199 chr21:45148571-45148578 chr21:45148568-45148583 chr21:45148570-45148579 chr21:45148570-45148580 chr21:45148533-45148542 chr21:45148532-45148539 chr21:45148531-45148541

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45148864-45148914	PANC-1	pancreas:	n/a
2	chr21:45148879-45148929	HCM	heart:	n/a
3	chr21:45148879-45148929	HPAEpiC	pulmonary alveolar:	n/a
4	chr21:45148864-45148914	A549	lung:	n/a
5	chr21:45148879-45148929	A549	lung:	n/a
6	chr21:45148879-45148929	RPTEC	kidney:	n/a
7	chr21:45148864-45148914	BE2_C	brain:	n/a
8	chr21:45148864-45148914	IMR90	lung:	fetal
9	chr21:45148864-45148914	ECC-1	luminal epithelium:	n/a
10	chr21:45148879-45148929	MCF10A-Er-Src	breast:	n/a
11	chr21:45148864-45148914	NT2-D1	testis:	n/a
12	chr21:45148879-45148929	U87	brain:	n/a
13	chr21:45148864-45148914	AG10803	skin:	n/a
14	chr21:45148864-45148914	GM12878	blood:	n/a
15	chr21:45148864-45148914	HCM	heart:	n/a
16	chr21:45148864-45148914	HCT-116	colon:	n/a
17	chr21:45148864-45148914	HUVEC	blood vessel:	n/a
18	chr21:45148864-45148914	HIPEpiC	eye:	n/a
19	chr21:45148864-45148914	U87	brain:	n/a
20	chr21:45148879-45148929	PrEC	prostate:	n/a
21	chr21:45148879-45148929	ProgFib	skin:	n/a
22	chr21:45148864-45148914	SAEC	small airway:	n/a
23	chr21:45148879-45148929	NT2-D1	testis:	n/a
24	chr21:45148879-45148929	IMR90	lung:	fetal
25	chr21:45148879-45148929	BE2_C	brain:	n/a
26	chr21:45148879-45148929	HL-60	blood:	n/a
27	chr21:45148864-45148914	NB4	blood:	n/a
28	chr21:45148864-45148914	HRPEpiC	eye:	n/a
29	chr21:45148879-45148929	AG04450	lung:	fetal
30	chr21:45148864-45148914	LNCaP	prostate:	n/a
31	chr21:45148879-45148929	MCF-7	breast:	n/a
32	chr21:45148864-45148914	NHBE	bronchial:	n/a
33	chr21:45148864-45148914	HEEpiC	esophagus:	n/a
34	chr21:45148864-45148914	AG09309	skin:	n/a
35	chr21:45148864-45148914	HCF	heart:	n/a
36	chr21:45148879-45148929	HRCEpiC	kidney:	n/a
37	chr21:45148864-45148914	GM06990	blood:	n/a
38	chr21:45148864-45148914	NHDF-neo	bronchial:	n/a
39	chr21:45148879-45148929	HCT-116	colon:	n/a
40	chr21:45148879-45148929	AoSMC	blood vessel:	n/a
41	chr21:45148879-45148929	NHDF-neo	bronchial:	n/a
42	chr21:45148879-45148929	HIPEpiC	eye:	n/a
43	chr21:45148864-45148914	BJ	skin:	n/a
44	chr21:45148879-45148929	Hela-S3	cervix:	n/a
45	chr21:45148879-45148929	ovcar-3	ovarian:	n/a
46	chr21:45148864-45148914	GM12891	blood:	n/a
47	chr21:45148864-45148914	ProgFib	skin:	n/a
48	chr21:45148864-45148914	HRCEpiC	kidney:	n/a
49	chr21:45148864-45148914	CMK	blood:	n/a
50	chr21:45148879-45148929	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:45147195..45149472-chr21:45196303..45198972,2	K562	blood:
2	chr21:45147353..45150091-chr21:45163613..45167274,4	K562	blood:
3	chr21:44297829..44300678-chr21:45147311..45150231,2	K562	blood:
4	chr21:45138878..45139799-chr21:45148124..45149007,3	K562	blood:
5	chr21:45146930..45150669-chr21:45163613..45169103,5	K562	blood:

Variant related genes	Relation type
PDXK	TF binding region
PDXK	CpG island
ENSG00000160194	Chromatin interaction
ENSG00000160213	Chromatin interaction
ENSG00000160209	Chromatin interaction
ENSG00000160193	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv913874	chr21:45041790-45191005	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv531544	chr21:45071371-45202912	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv531545	chr21:45095397-45395904	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	esv3424986	chr21:45118675-45158421	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	esv3329872	chr21:45118725-45158757	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv913875	chr21:45119629-45191005	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv913876	chr21:45119629-45267193	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
8	nsv587701	chr21:45128190-45181446	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv459290	chr21:45128454-45191139	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
10	nsv587702	chr21:45128454-45191139	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
11	nsv913877	chr21:45133868-45163689	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
12	nsv913878	chr21:45133868-45170285	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
13	esv2830066	chr21:45133868-45258047	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
14	esv1828675	chr21:45142427-45191139	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
15	nsv913879	chr21:45145286-45237039	Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv913880	chr21:45145286-45263920	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
17	nsv913881	chr21:45145286-45267193	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
18	nsv1055154	chr21:45148076-45203162	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45145200-45149400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr21:45145200-45149600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr21:45146000-45163600	Weak transcription	Dnd41	blood
4	chr21:45146600-45149400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr21:45146600-45149400	Enhancers	Small Intestine	intestine
6	chr21:45146600-45149600	Flanking Active TSS	Adipose Nuclei	Adipose
7	chr21:45146600-45149600	Enhancers	Gastric	stomach
8	chr21:45146800-45149400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr21:45146800-45149600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr21:45147000-45149200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
11	chr21:45147400-45149600	Flanking Active TSS	Duodenum Mucosa	Duodenum
12	chr21:45147400-45149600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr21:45147400-45149600	Flanking Active TSS	Stomach Smooth Muscle	stomach
14	chr21:45147600-45149200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
15	chr21:45147800-45149000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr21:45147800-45149200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
17	chr21:45147800-45149400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr21:45147800-45149400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr21:45147800-45149600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
20	chr21:45148000-45149200	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr21:45148000-45149200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
22	chr21:45148000-45149200	Flanking Active TSS	Fetal Muscle Trunk	muscle
23	chr21:45148000-45149400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr21:45148000-45149400	Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr21:45148000-45149600	Active TSS	H9 Cell Line	embryonic stem cell
26	chr21:45148000-45149600	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr21:45148000-45149600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr21:45148000-45149600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr21:45148000-45149600	Flanking Active TSS	Fetal Muscle Leg	muscle
30	chr21:45148000-45149600	Flanking Active TSS	Placenta	Placenta
31	chr21:45148000-45149600	Flanking Active TSS	HMEC	breast
32	chr21:45148000-45149800	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr21:45148200-45149000	Active TSS	Brain Angular Gyrus	brain
34	chr21:45148200-45149000	Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr21:45148200-45149000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
36	chr21:45148200-45149200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr21:45148200-45149200	Flanking Active TSS	Fetal Brain Male	brain
38	chr21:45148200-45149200	Active TSS	Ovary	ovary
39	chr21:45148200-45149200	Active TSS	Right Atrium	heart
40	chr21:45148200-45149400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr21:45148200-45149400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr21:45148200-45149400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr21:45148200-45149400	Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr21:45148200-45149400	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr21:45148200-45149400	Flanking Active TSS	Liver	Liver
46	chr21:45148200-45149600	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr21:45148200-45149600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr21:45148200-45149600	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr21:45148200-45149800	Active TSS	iPS-18 Cell Line	embryonic stem cell
50	chr21:45148200-45149800	Active TSS	Fetal Kidney	kidney

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