Variant report

Variant	rs2941511
Chromosome Location	chr17:37820175-37820176
allele	C/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	chr17:37819935-37820670	H1-hESC	embryonic stem cell:	n/a	n/a
2	YY1	chr17:37820130-37820262	K562	blood:	n/a	n/a
3	POLR2A	chr17:37819888-37820416	HCT-116	colon:	n/a	n/a
4	MAZ	chr17:37819367-37820899	IMR90	lung:	n/a	chr17:37819743-37819753 chr17:37820491-37820500 chr17:37819965-37819975 chr17:37820490-37820501 chr17:37819889-37819899 chr17:37820492-37820499 chr17:37820490-37820500 chr17:37820489-37820504
5	POLR2A	chr17:37820067-37820303	HepG2	liver:	n/a	n/a
6	YY1	chr17:37819867-37820392	H1-hESC	embryonic stem cell:	n/a	chr17:37819960-37819969 chr17:37819887-37819896
7	SIN3A	chr17:37819978-37820538	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr17:37820137-37820388	GM12878	blood:	n/a	n/a
9	CTCF	chr17:37820140-37820290	WERI-Rb-1	eye:	n/a	n/a
10	BACH1	chr17:37820027-37820211	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr17:37819970-37820428	ECC-1	luminal epithelium:	n/a	n/a
12	POLR2A	chr17:37819835-37822433	K562	blood:	n/a	n/a
13	HEY1	chr17:37819909-37820309	K562	blood:	n/a	chr17:37819973-37819988
14	POLR2A	chr17:37819881-37820866	ECC-1	luminal epithelium:	n/a	n/a
15	POLR2A	chr17:37820017-37820257	Hela-S3	cervix:	n/a	n/a
16	MAX	chr17:37820145-37820549	K562	blood:	n/a	chr17:37820491-37820500 chr17:37820490-37820501 chr17:37820492-37820499 chr17:37820490-37820500 chr17:37820489-37820504
17	YY1	chr17:37819905-37820373	H1-hESC	embryonic stem cell:	n/a	chr17:37819960-37819969
18	POLR2A	chr17:37820040-37820266	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr17:37819937-37822773	K562	blood:	n/a	n/a
20	CHD2	chr17:37820120-37820281	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr17:37819944-37820354	A549	lung:	n/a	n/a
22	TCF12	chr17:37819782-37820710	ECC-1	luminal epithelium:	n/a	n/a
23	JUND	chr17:37820013-37820477	K562	blood:	n/a	n/a
24	BCL3	chr17:37819921-37821125	A549	lung:	n/a	n/a
25	CTBP2	chr17:37819972-37820384	H1-hESC	embryonic stem cell:	n/a	n/a
26	HEY1	chr17:37819938-37820220	K562	blood:	n/a	chr17:37819973-37819988
27	SP1	chr17:37819875-37820419	H1-hESC	embryonic stem cell:	n/a	chr17:37819958-37819970 chr17:37819959-37819968 chr17:37819890-37819899 chr17:37820214-37820223 chr17:37819888-37819900 chr17:37820212-37820224 chr17:37819959-37819973 chr17:37819959-37819969 chr17:37819958-37819970 chr17:37819889-37819899 chr17:37819888-37819900 chr17:37819959-37819968 chr17:37819889-37819898 chr17:37819959-37819969 chr17:37819889-37819903 chr17:37819960-37819969 chr17:37820011-37820025 chr17:37820212-37820224
28	ZBTB7A	chr17:37818112-37820811	ECC-1	luminal epithelium:	n/a	chr17:37818475-37818489
29	POLR2A	chr17:37819920-37822310	SK-N-MC	brain:	n/a	n/a
30	POLR2A	chr17:37820128-37820328	GM12878	blood:	n/a	n/a
31	KAP1	chr17:37820094-37820548	HEK293	kidney:	n/a	n/a
32	POLR2A	chr17:37819928-37825272	K562	blood:	n/a	n/a
33	TCF12	chr17:37818523-37820614	ECC-1	luminal epithelium:	n/a	n/a
34	UBTF	chr17:37820063-37820388	K562	blood:	n/a	n/a
35	POLR2A	chr17:37820027-37820333	A549	lung:	n/a	n/a
36	CTCF	chr17:37820135-37820327	K562	blood:	n/a	n/a
37	MAZ	chr17:37820112-37820373	HepG2	liver:	n/a	n/a
38	POLR2A	chr17:37819929-37820376	A549	lung:	n/a	n/a
39	MAZ	chr17:37819896-37820691	K562	blood:	n/a	chr17:37820491-37820500 chr17:37819965-37819975 chr17:37820490-37820501 chr17:37820492-37820499 chr17:37820490-37820500 chr17:37820489-37820504
40	MAX	chr17:37819893-37820681	ECC-1	luminal epithelium:	n/a	chr17:37820491-37820500 chr17:37819965-37819975 chr17:37820490-37820501 chr17:37820492-37820499 chr17:37820490-37820500 chr17:37820489-37820504
41	RCOR1	chr17:37820032-37820868	K562	blood:	n/a	n/a
42	POLR2A	chr17:37820034-37820371	Hela-S3	cervix:	n/a	n/a
43	EP300	chr17:37819854-37820736	ECC-1	luminal epithelium:	n/a	chr17:37819900-37819913
44	POLR2A	chr17:37819910-37820482	K562	blood:	n/a	n/a
45	UBTF	chr17:37820021-37820391	K562	blood:	n/a	n/a
46	POLR2A	chr17:37820082-37821403	HepG2	liver:	n/a	n/a
47	ELF1	chr17:37819991-37820358	K562	blood:	n/a	n/a
48	MAX	chr17:37820128-37820323	A549	lung:	n/a	n/a
49	CTCF	chr17:37820120-37820270	HEK293	kidney:	n/a	n/a
50	POLR2A	chr17:37820098-37820418	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:37820135-37820185	GM06990	blood:	n/a
2	chr17:37820135-37820185	A549	lung:	n/a
3	chr17:37820135-37820185	ECC-1	luminal epithelium:	n/a
4	chr17:37820135-37820185	GM12891	blood:	n/a
5	chr17:37820135-37820185	HCT-116	colon:	n/a
6	chr17:37820135-37820185	SK-N-MC	brain:	n/a
7	chr17:37820135-37820185	PrEC	prostate:	n/a
8	chr17:37820135-37820185	HRE	kidney:	n/a
9	chr17:37820135-37820185	NHDF-neo	bronchial:	n/a
10	chr17:37820135-37820185	NH-A	brain:	n/a
11	chr17:37820135-37820185	AG04450	lung:	fetal
12	chr17:37820135-37820185	K562	blood:	n/a
13	chr17:37820135-37820185	HRPEpiC	eye:	n/a
14	chr17:37820135-37820185	HepG2	liver:	n/a
15	chr17:37820135-37820185	HUVEC	blood vessel:	n/a
16	chr17:37820135-37820185	NHBE	bronchial:	n/a
17	chr17:37820135-37820185	T-47D	breast:	n/a
18	chr17:37820135-37820185	Caco-2	colon:	n/a
19	chr17:37820135-37820185	BJ	skin:	n/a
20	chr17:37820135-37820185	Jurkat	blood:	n/a
21	chr17:37820135-37820185	GM12878	blood:	n/a
22	chr17:37820135-37820185	CMK	blood:	n/a
23	chr17:37820135-37820185	HIPEpiC	eye:	n/a
24	chr17:37820135-37820185	HL-60	blood:	n/a
25	chr17:37820135-37820185	PANC-1	pancreas:	n/a
26	chr17:37820135-37820185	Hela-S3	cervix:	n/a
27	chr17:37820135-37820185	HRCEpiC	kidney:	n/a
28	chr17:37820135-37820185	HCF	heart:	n/a
29	chr17:37820135-37820185	HCPEpiC	choroid plexus:	n/a
30	chr17:37820135-37820185	AoSMC	blood vessel:	n/a
31	chr17:37820135-37820185	NB4	blood:	n/a
32	chr17:37820135-37820185	MCF10A-Er-Src	breast:	n/a
33	chr17:37820135-37820185	BE2_C	brain:	n/a
34	chr17:37820135-37820185	U87	brain:	n/a
35	chr17:37820135-37820185	LNCaP	prostate:	n/a
36	chr17:37820135-37820185	Hepatocyte	liver:	n/a
37	chr17:37820135-37820185	MCF-7	breast:	n/a
38	chr17:37820135-37820185	AG09309	skin:	n/a
39	chr17:37820135-37820185	AG10803	skin:	n/a
40	chr17:37820135-37820185	ProgFib	skin:	n/a
41	chr17:37820135-37820185	ovcar-3	ovarian:	n/a
42	chr17:37820135-37820185	HNPCEpiC	eye:	n/a
43	chr17:37820135-37820185	AG04449	skin:	fetal
44	chr17:37820135-37820185	HEK293	kidney:	embryo
45	chr17:37820135-37820185	HAEpiC	amniotic membrane:	n/a
46	chr17:37820135-37820185	AG09319	gingival:	n/a
47	chr17:37820135-37820185	HCM	heart:	n/a
48	chr17:37820135-37820185	RPTEC	kidney:	n/a
49	chr17:37820135-37820185	SKMC	muscle:	n/a
50	chr17:37820135-37820185	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:37814865..37817539-chr17:37818088..37820916,2	MCF-7	breast:
2	chr17:37818282..37821110-chr17:37882752..37884709,2	K562	blood:
3	chr17:37820151..37821695-chr17:37885037..37886831,2	K562	blood:
4	chr17:37773404..37776321-chr17:37819728..37822241,2	MCF-7	breast:
5	chr17:37777756..37783081-chr17:37819129..37825010,9	K562	blood:
6	chr17:37820097..37822634-chr17:37895456..37897611,2	K562	blood:
7	chr17:37790905..37794856-chr17:37820000..37822270,4	K562	blood:

Variant related genes	Relation type
PNMT	TF binding region
TCAP	TF binding region
TCAP	CpG island
PNMT	CpG island
ENSG00000141736	Chromatin interaction
ENSG00000141738	Chromatin interaction
ENSG00000214546	Chromatin interaction
ENSG00000131748	Chromatin interaction
ENSG00000131771	Chromatin interaction
ENSG00000141741	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1050293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs15968	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934958	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934959	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934960	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934961	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934965	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934966	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2941510	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941512	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941514	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941515	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941516	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2941523	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2952139	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2952149	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2952150	0.92[EUR][1000 genomes]
rs57837184	0.84[AFR][1000 genomes]
rs59522915	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294088	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294092	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294095	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73294098	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73296106	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73296109	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73308326	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv516757	chr17:37781849-37834541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
11	esv1792029	chr17:37797757-37886460	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv908213	chr17:37807698-37839493	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
13	nsv528093	chr17:37814080-37866005	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
14	nsv908214	chr17:37814224-37861833	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv574992	chr17:37818561-37822311	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
16	nsv908215	chr17:37818561-37834541	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37795000-37823800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr17:37803800-37821800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr17:37810000-37820400	Strong transcription	Brain Germinal Matrix	brain
4	chr17:37810600-37821000	Weak transcription	Fetal Brain Male	brain
5	chr17:37810800-37820600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr17:37811800-37820800	Strong transcription	Fetal Brain Female	brain
7	chr17:37813000-37820800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr17:37814000-37820400	Genic enhancers	Fetal Muscle Trunk	muscle
9	chr17:37816600-37821600	Enhancers	Psoas Muscle	Psoas
10	chr17:37816800-37820800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:37817000-37820200	Weak transcription	HUVEC	blood vessel
12	chr17:37817000-37823000	Weak transcription	GM12878-XiMat	blood
13	chr17:37817200-37821000	Enhancers	Fetal Heart	heart
14	chr17:37817600-37823400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr17:37818000-37820200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr17:37818000-37821200	Genic enhancers	Esophagus	oesophagus
17	chr17:37818200-37820400	Weak transcription	Brain Angular Gyrus	brain
18	chr17:37818200-37821000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr17:37818200-37823000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr17:37818400-37821800	Weak transcription	Colon Smooth Muscle	Colon
21	chr17:37818400-37823600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr17:37818600-37820400	Weak transcription	Rectal Smooth Muscle	rectum
23	chr17:37818600-37821000	Genic enhancers	Fetal Intestine Small	intestine
24	chr17:37818600-37821000	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr17:37818600-37821800	Weak transcription	Primary B cells from cord blood	blood
26	chr17:37818600-37822000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr17:37818800-37820200	Strong transcription	Thymus	Thymus
28	chr17:37818800-37820600	Enhancers	Right Atrium	heart
29	chr17:37818800-37820800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr17:37818800-37821200	Genic enhancers	Brain Cingulate Gyrus	brain
31	chr17:37818800-37821600	Enhancers	Stomach Mucosa	stomach
32	chr17:37819000-37820600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr17:37819200-37820600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr17:37819200-37821000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr17:37819200-37821000	Enhancers	Stomach Smooth Muscle	stomach
36	chr17:37819200-37822000	Enhancers	Colonic Mucosa	Colon
37	chr17:37819200-37822200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr17:37819200-37822200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr17:37819200-37825200	Enhancers	Liver	Liver
40	chr17:37819400-37820200	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr17:37819400-37820400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr17:37819400-37821000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr17:37819400-37821400	Enhancers	Duodenum Mucosa	Duodenum
44	chr17:37819400-37821400	Enhancers	Fetal Intestine Large	intestine
45	chr17:37819400-37821600	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr17:37819400-37822000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr17:37819400-37822000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr17:37819400-37822000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr17:37819400-37822000	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr17:37819400-37822200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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