Variant report

Variant	rs17700839
Chromosome Location	chr17:45899057-45899058
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:305)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:305 , 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	ELF1	chr17:45898881-45899426	HepG2	liver:	n/a	n/a
2	ELF1	chr17:45898390-45899398	GM12878	blood:	n/a	n/a
3	POLR2A	chr17:45898880-45899417	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr17:45898841-45899374	GM12892	blood:	n/a	n/a
5	E2F4	chr17:45899045-45899362	MCF10A-Er-Src	breast:	n/a	n/a
6	MAZ	chr17:45898986-45899610	Hela-S3	cervix:	n/a	chr17:45899471-45899481
7	YY1	chr17:45898619-45899296	GM12892	blood:	n/a	n/a
8	CCNT2	chr17:45898990-45899374	K562	blood:	n/a	n/a
9	MAZ	chr17:45898763-45899472	K562	blood:	n/a	n/a
10	YY1	chr17:45898875-45899269	K562	blood:	n/a	n/a
11	TBP	chr17:45898919-45899352	K562	blood:	n/a	n/a
12	SIN3AK20	chr17:45898896-45899459	A549	lung:	n/a	n/a
13	POLR2A	chr17:45898899-45899369	HepG2	liver:	n/a	n/a
14	POLR2A	chr17:45898858-45899399	Gliobla	brain:	n/a	n/a
15	POLR2A	chr17:45898896-45899451	GM18951	blood:	n/a	n/a
16	POLR2A	chr17:45898752-45899887	GM12878	blood:	n/a	n/a
17	TCF12	chr17:45898990-45899216	GM12878	blood:	n/a	n/a
18	GTF2F1	chr17:45898930-45899390	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr17:45898899-45899359	HepG2	liver:	n/a	n/a
20	MAX	chr17:45898823-45899522	SK-N-SH	brain:	n/a	chr17:45899471-45899481
21	MAX	chr17:45898858-45899469	SK-N-SH	brain:	n/a	n/a
22	TAF1	chr17:45898867-45899393	HepG2	liver:	n/a	n/a
23	SIN3AK20	chr17:45898926-45899287	HepG2	liver:	n/a	n/a
24	REST	chr17:45898545-45899271	A549	lung:	n/a	chr17:45898919-45898932 chr17:45899128-45899141 chr17:45899199-45899212
25	POU2F2	chr17:45898904-45899453	GM12878	blood:	n/a	chr17:45899257-45899269 chr17:45898936-45898948
26	GABPA	chr17:45898945-45899429	A549	lung:	n/a	n/a
27	POLR2A	chr17:45898757-45899492	Hela-S3	cervix:	n/a	n/a
28	PAX5	chr17:45898947-45899443	GM12878	blood:	n/a	n/a
29	POLR2A	chr17:45898859-45899376	HUVEC	blood vessel:	n/a	n/a
30	EP300	chr17:45899014-45899354	K562	blood:	n/a	n/a
31	HDAC2	chr17:45898806-45899433	HepG2	liver:	n/a	n/a
32	JUN	chr17:45898622-45899917	K562	blood:	n/a	chr17:45899081-45899091 chr17:45899081-45899091 chr17:45899078-45899089 chr17:45899081-45899091 chr17:45899081-45899091 chr17:45899467-45899476 chr17:45899082-45899090
33	HCFC1	chr17:45898915-45899423	K562	blood:	n/a	n/a
34	REST	chr17:45898935-45899481	PFSK-1	brain:	n/a	chr17:45899128-45899141 chr17:45899199-45899212
35	ZBTB7A	chr17:45898793-45899437	K562	blood:	n/a	n/a
36	POLR2A	chr17:45898869-45899352	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:45898273-45900544	SK-N-SH	brain:	n/a	chr17:45899669-45899676
38	POLR2A	chr17:45898915-45899477	GM19099	blood:	n/a	n/a
39	TAF1	chr17:45898924-45899469	SK-N-SH	brain:	n/a	n/a
40	POLR2A	chr17:45898934-45899356	A549	lung:	n/a	n/a
41	ZNF263	chr17:45898412-45901267	HEK293-T-REx	kidney:	n/a	chr17:45899220-45899229 chr17:45899206-45899227
42	YY1	chr17:45898953-45899400	A549	lung:	n/a	n/a
43	POLR2A	chr17:45898844-45899422	HUVEC	blood vessel:	n/a	n/a
44	MTA3	chr17:45898764-45899495	GM12878	blood:	n/a	n/a
45	ETS1	chr17:45898978-45899314	K562	blood:	n/a	n/a
46	SIN3AK20	chr17:45898975-45899295	HepG2	liver:	n/a	n/a
47	ZNF384	chr17:45898836-45899377	K562	blood:	n/a	n/a
48	POLR2A	chr17:45898934-45899433	GM12891	blood:	n/a	n/a
49	ELF1	chr17:45898861-45899479	SK-N-SH	brain:	n/a	chr17:45899466-45899478
50	MYC	chr17:45898960-45899344	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45899047-45899097	HCM	heart:	n/a
2	chr17:45899047-45899097	SK-N-MC	brain:	n/a
3	chr17:45899047-45899097	NH-A	brain:	n/a
4	chr17:45899047-45899097	AG09319	gingival:	n/a
5	chr17:45899047-45899097	NHDF-neo	bronchial:	n/a
6	chr17:45899047-45899097	IMR90	lung:	fetal
7	chr17:45899047-45899097	HRE	kidney:	n/a
8	chr17:45899047-45899097	Caco-2	colon:	n/a
9	chr17:45899047-45899097	H1-hESC	embryonic stem cell:	embryo
10	chr17:45899047-45899097	BE2_C	brain:	n/a
11	chr17:45899047-45899097	GM19239	blood:	n/a
12	chr17:45899047-45899097	U87	brain:	n/a
13	chr17:45899047-45899097	HCF	heart:	n/a
14	chr17:45899047-45899097	SAEC	small airway:	n/a
15	chr17:45899047-45899097	PFSK-1	brain:	n/a
16	chr17:45899047-45899097	RPTEC	kidney:	n/a
17	chr17:45899047-45899097	SK-N-SH	brain:	n/a
18	chr17:45899047-45899097	NHBE	bronchial:	n/a
19	chr17:45899047-45899097	HRCEpiC	kidney:	n/a
20	chr17:45899047-45899097	LNCaP	prostate:	n/a
21	chr17:45899047-45899097	GM06990	blood:	n/a
22	chr17:45899047-45899097	ProgFib	skin:	n/a
23	chr17:45899047-45899097	CMK	blood:	n/a
24	chr17:45899047-45899097	GM12891	blood:	n/a
25	chr17:45899047-45899097	HPAEpiC	pulmonary alveolar:	n/a
26	chr17:45899047-45899097	SK-N-SH_RA	brain:	n/a
27	chr17:45899047-45899097	HEEpiC	esophagus:	n/a
28	chr17:45899047-45899097	K562	blood:	n/a
29	chr17:45899047-45899097	Hela-S3	cervix:	n/a
30	chr17:45899047-45899097	HRPEpiC	eye:	n/a
31	chr17:45899047-45899097	HCPEpiC	choroid plexus:	n/a
32	chr17:45899047-45899097	HepG2	liver:	n/a
33	chr17:45899047-45899097	ECC-1	luminal epithelium:	n/a
34	chr17:45899047-45899097	T-47D	breast:	n/a
35	chr17:45899047-45899097	MCF-7	breast:	n/a
36	chr17:45899047-45899097	GM12892	blood:	n/a
37	chr17:45899047-45899097	HCT-116	colon:	n/a
38	chr17:45899047-45899097	AG04450	lung:	fetal
39	chr17:45899047-45899097	MCF10A-Er-Src	breast:	n/a
40	chr17:45899047-45899097	PANC-1	pancreas:	n/a
41	chr17:45899047-45899097	HIPEpiC	eye:	n/a
42	chr17:45899047-45899097	NB4	blood:	n/a
43	chr17:45899047-45899097	AG10803	skin:	n/a
44	chr17:45899047-45899097	HNPCEpiC	eye:	n/a
45	chr17:45899047-45899097	Hepatocyte	liver:	n/a
46	chr17:45899047-45899097	AoSMC	blood vessel:	n/a
47	chr17:45899047-45899097	AG04449	skin:	fetal
48	chr17:45899047-45899097	PrEC	prostate:	n/a
49	chr17:45899047-45899097	HL-60	blood:	n/a
50	chr17:45899047-45899097	A549	lung:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45897420..45900355-chr17:45972655..45975500,3	MCF-7	breast:
2	chr17:45897077..45901616-chr17:45914627..45919028,8	MCF-7	breast:
3	chr17:45897782..45899976-chr17:46017642..46019403,2	MCF-7	breast:
4	chr17:45895199..45899793-chr17:45971655..45976847,6	K562	blood:
5	chr17:45886192..45893448-chr17:45896148..45900071,14	MCF-7	breast:
6	chr17:45897542..45899776-chr17:45916869..45918658,2	MCF-7	breast:
7	chr17:45894310..45903569-chr17:45906761..45911816,14	MCF-7	breast:
8	chr17:45898761..45899596-chr17:45908446..45908960,2	MCF-7	breast:
9	chr17:45898563..45901614-chr17:46033321..46036165,3	MCF-7	breast:

No data

Variant related genes	Relation type
OSBPL7	TF binding region
OSBPL7	CpG island
ENSG00000141294	Chromatin interaction
ENSG00000108439	Chromatin interaction
ENSG00000006025	Chromatin interaction
ENSG00000264920	Chromatin interaction
ENSG00000141295	Chromatin interaction
ENSG00000167182	Chromatin interaction
ENSG00000159111	Chromatin interaction
ENSG00000167183	Chromatin interaction
ENSG00000234494	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1004770	0.95[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1053800	0.91[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11538867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11650451	1.00[CHB][hapmap]
rs16947078	1.00[CHB][hapmap]
rs17035	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17700574	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17700604	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17701022	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17701113	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17773860	0.95[CEU][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17774008	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17774144	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17774166	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17774171	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs17774272	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs2051761	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2106800	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2277693	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2301690	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3209	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55791443	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55840099	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55928544	0.90[EUR][1000 genomes]
rs55998645	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56156511	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076104	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076125	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076126	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076127	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076129	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076131	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076132	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076133	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076135	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62076137	1.00[ASN][1000 genomes]
rs62076138	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72833429	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72833439	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs729988	0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs732840	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8064399	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8077844	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs878295	1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9898606	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498122	chr17:45763853-46064327	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv908572	chr17:45858487-45900856	Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv908573	chr17:45858487-45956073	Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv908574	chr17:45876022-45930584	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv517880	chr17:45887951-45933341	Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	22 gene(s)	inside rSNPs	diseases
6	nsv518892	chr17:45887951-46029432	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17700839	LRRC46	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45896400-45901000	Weak transcription	Aorta	Aorta
2	chr17:45897400-45899400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:45897400-45899400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr17:45897400-45899800	Flanking Active TSS	Duodenum Mucosa	Duodenum
5	chr17:45897400-45900000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
6	chr17:45897800-45899400	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr17:45897800-45899400	Active TSS	Stomach Mucosa	stomach
8	chr17:45897800-45899600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
9	chr17:45897800-45899600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
10	chr17:45897800-45899800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr17:45897800-45899800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr17:45898000-45899600	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr17:45898000-45899600	Flanking Active TSS	Primary T cells from cord blood	blood
14	chr17:45898000-45899600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
15	chr17:45898000-45899600	Flanking Active TSS	Brain Germinal Matrix	brain
16	chr17:45898000-45899600	Flanking Active TSS	Fetal Muscle Trunk	muscle
17	chr17:45898000-45899600	Flanking Active TSS	Fetal Muscle Leg	muscle
18	chr17:45898000-45899800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
19	chr17:45898000-45899800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr17:45898000-45899800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr17:45898000-45899800	Flanking Active TSS	Stomach Smooth Muscle	stomach
22	chr17:45898200-45899200	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr17:45898200-45899400	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr17:45898200-45899400	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr17:45898200-45899600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr17:45898200-45899600	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr17:45898200-45899600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr17:45898200-45899600	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr17:45898200-45899600	Active TSS	Small Intestine	intestine
30	chr17:45898200-45899800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr17:45898200-45899800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr17:45898200-45899800	Flanking Active TSS	HMEC	breast
33	chr17:45898200-45900200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr17:45898400-45899200	Flanking Active TSS	Right Ventricle	heart
35	chr17:45898400-45899400	Active TSS	H9 Cell Line	embryonic stem cell
36	chr17:45898400-45899400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr17:45898400-45899400	Active TSS	Fetal Kidney	kidney
38	chr17:45898400-45899400	Active TSS	GM12878-XiMat	blood
39	chr17:45898400-45899400	Active TSS	NHLF	lung
40	chr17:45898400-45899600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr17:45898400-45899600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
42	chr17:45898400-45899600	Flanking Active TSS	Primary B cells from peripheral blood	blood
43	chr17:45898400-45899600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
44	chr17:45898400-45899600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr17:45898400-45899600	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr17:45898400-45899600	Flanking Active TSS	Fetal Brain Female	brain
47	chr17:45898400-45899600	Flanking Active TSS	Right Atrium	heart
48	chr17:45898400-45899800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr17:45898400-45899800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr17:45898400-45899800	Flanking Active TSS	Adipose Nuclei	Adipose

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