Variant report

Variant	rs1549760
Chromosome Location	chr7:150755839-150755840
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	chr7:150754493-150760694	K562	blood:	n/a	n/a
2	MAX	chr7:150754709-150756211	A549	lung:	n/a	chr7:150756001-150756008 chr7:150755999-150756012 chr7:150755999-150756012 chr7:150755996-150756015 chr7:150756003-150756010
3	CREB1	chr7:150754483-150756028	K562	blood:	n/a	n/a
4	MAX	chr7:150754773-150756263	ECC-1	luminal epithelium:	n/a	chr7:150756001-150756008 chr7:150755999-150756012 chr7:150755999-150756012 chr7:150755996-150756015 chr7:150756003-150756010
5	TCF7L2	chr7:150754907-150755855	Hela-S3	cervix:	n/a	chr7:150755283-150755297
6	YY1	chr7:150754635-150755855	K562	blood:	n/a	n/a
7	STAT5A	chr7:150754644-150756103	K562	blood:	n/a	chr7:150755855-150755867
8	POLR2A	chr7:150754758-150760600	K562	blood:	n/a	n/a
9	SIN3AK20	chr7:150754689-150755895	MCF-7	breast:	n/a	n/a
10	MXI1	chr7:150754711-150756196	GM12878	blood:	n/a	n/a
11	EP300	chr7:150754771-150755903	ECC-1	luminal epithelium:	n/a	n/a
12	MYC	chr7:150754647-150758067	K562	blood:	n/a	chr7:150756001-150756008 chr7:150755999-150756012 chr7:150755999-150756012 chr7:150757089-150757099 chr7:150755996-150756015 chr7:150756003-150756010
13	POLR2A	chr7:150754556-150755861	PFSK-1	brain:	n/a	n/a
14	IRF1	chr7:150754763-150757149	K562	blood:	n/a	chr7:150755018-150755032
15	POLR2A	chr7:150754631-150757369	HUVEC	blood vessel:	n/a	n/a
16	SREBP1	chr7:150754410-150757606	GM12878	blood:	n/a	n/a
17	NR2F2	chr7:150753155-150758025	K562	blood:	n/a	n/a
18	MAFK	chr7:150754659-150756117	K562	blood:	n/a	n/a
19	RUNX3	chr7:150754767-150756095	GM12878	blood:	n/a	n/a
20	POLR2A	chr7:150754724-150758316	U87	brain:	n/a	n/a
21	MXI1	chr7:150754410-150760844	IMR90	lung:	n/a	chr7:150759550-150759559 chr7:150759552-150759561 chr7:150760584-150760593 chr7:150759552-150759561
22	POLR2A	chr7:150754701-150757473	HUVEC	blood vessel:	n/a	n/a
23	ATF1	chr7:150754903-150756040	K562	blood:	n/a	n/a
24	POLR2A	chr7:150754770-150755965	GM19193	blood:	n/a	n/a
25	MAX	chr7:150754617-150756339	ECC-1	luminal epithelium:	n/a	chr7:150756001-150756008 chr7:150755999-150756012 chr7:150755999-150756012 chr7:150755996-150756015 chr7:150756003-150756010
26	POLR2A	chr7:150754600-150756007	K562	blood:	n/a	n/a
27	ZC3H11A	chr7:150754650-150756069	K562	blood:	n/a	n/a
28	POLR2A	chr7:150754086-150757415	HepG2	liver:	n/a	n/a
29	PML	chr7:150754752-150755952	K562	blood:	n/a	n/a
30	SIN3A	chr7:150753793-150756399	H1-hESC	embryonic stem cell:	n/a	n/a
31	TCF7L2	chr7:150754740-150756091	HEK293	kidney:	n/a	chr7:150755283-150755297
32	POLR2A	chr7:150754259-150757131	Raji	blood:	n/a	n/a
33	ELK1	chr7:150755809-150755860	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr7:150755184-150756047	ProgFib	skin:	n/a	n/a
35	POLR2A	chr7:150754772-150758468	U87	brain:	n/a	n/a
36	POLR2A	chr7:150755164-150755844	H1-hESC	embryonic stem cell:	n/a	n/a
37	JUN	chr7:150754811-150755947	K562	blood:	n/a	n/a
38	POLR2A	chr7:150754996-150755983	GM12892	blood:	n/a	n/a
39	POLR2A	chr7:150754766-150758468	U87	brain:	n/a	n/a
40	POLR2A	chr7:150754806-150760313	K562	blood:	n/a	n/a
41	POLR2A	chr7:150754523-150760219	SK-N-MC	brain:	n/a	n/a
42	ZBTB7A	chr7:150755276-150755939	ECC-1	luminal epithelium:	n/a	n/a
43	E2F6	chr7:150755004-150756004	K562	blood:	n/a	chr7:150755942-150755957
44	CREB1	chr7:150754600-150758238	HepG2	liver:	n/a	n/a
45	ELF1	chr7:150754482-150755883	GM12878	blood:	n/a	n/a
46	HDAC2	chr7:150755008-150755885	K562	blood:	n/a	n/a
47	POLR2A	chr7:150754764-150756995	GM12891	blood:	n/a	n/a
48	MAX	chr7:150754965-150757371	K562	blood:	n/a	chr7:150756001-150756008 chr7:150755999-150756012 chr7:150755999-150756012 chr7:150757089-150757099 chr7:150755996-150756015 chr7:150756003-150756010
49	POLR2A	chr7:150754772-150755911	GM12892	blood:	n/a	n/a
50	SIN3AK20	chr7:150755432-150755980	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150755834-150755884	H1-hESC	embryonic stem cell:	embryo
2	chr7:150755834-150755884	GM12878	blood:	n/a
3	chr7:150755834-150755884	PrEC	prostate:	n/a
4	chr7:150755834-150755884	CMK	blood:	n/a
5	chr7:150755834-150755884	GM12892	blood:	n/a
6	chr7:150755834-150755884	IMR90	lung:	fetal
7	chr7:150755834-150755884	U87	brain:	n/a
8	chr7:150755834-150755884	AG10803	skin:	n/a
9	chr7:150755834-150755884	SK-N-SH_RA	brain:	n/a
10	chr7:150755834-150755884	K562	blood:	n/a
11	chr7:150755834-150755884	AG09319	gingival:	n/a
12	chr7:150755834-150755884	HepG2	liver:	n/a
13	chr7:150755834-150755884	AoSMC	blood vessel:	n/a
14	chr7:150755834-150755884	Caco-2	colon:	n/a
15	chr7:150755834-150755884	MCF10A-Er-Src	breast:	n/a
16	chr7:150755834-150755884	PANC-1	pancreas:	n/a
17	chr7:150755834-150755884	SKMC	muscle:	n/a
18	chr7:150755834-150755884	PFSK-1	brain:	n/a
19	chr7:150755834-150755884	HEEpiC	esophagus:	n/a
20	chr7:150755834-150755884	Hela-S3	cervix:	n/a
21	chr7:150755834-150755884	ovcar-3	ovarian:	n/a
22	chr7:150755834-150755884	ECC-1	luminal epithelium:	n/a
23	chr7:150755834-150755884	Hepatocyte	liver:	n/a
24	chr7:150755834-150755884	RPTEC	kidney:	n/a
25	chr7:150755834-150755884	BJ	skin:	n/a
26	chr7:150755834-150755884	SAEC	small airway:	n/a
27	chr7:150755834-150755884	GM12891	blood:	n/a
28	chr7:150755834-150755884	NB4	blood:	n/a
29	chr7:150755834-150755884	T-47D	breast:	n/a
30	chr7:150755834-150755884	AG04450	lung:	fetal
31	chr7:150755834-150755884	A549	lung:	n/a
32	chr7:150755834-150755884	SK-N-MC	brain:	n/a
33	chr7:150755834-150755884	GM19239	blood:	n/a
34	chr7:150755834-150755884	MCF-7	breast:	n/a
35	chr7:150755834-150755884	HCPEpiC	choroid plexus:	n/a
36	chr7:150755834-150755884	HAEpiC	amniotic membrane:	n/a
37	chr7:150755834-150755884	HIPEpiC	eye:	n/a
38	chr7:150755834-150755884	NT2-D1	testis:	n/a
39	chr7:150755834-150755884	LNCaP	prostate:	n/a
40	chr7:150755834-150755884	SK-N-SH	brain:	n/a
41	chr7:150755834-150755884	HMEC	breast:	n/a
42	chr7:150755834-150755884	HL-60	blood:	n/a
43	chr7:150755834-150755884	HRE	kidney:	n/a
44	chr7:150755834-150755884	HUVEC	blood vessel:	n/a
45	chr7:150755834-150755884	HRPEpiC	eye:	n/a
46	chr7:150755834-150755884	HCM	heart:	n/a
47	chr7:150755834-150755884	HCF	heart:	n/a
48	chr7:150755834-150755884	AG09309	skin:	n/a
49	chr7:150755834-150755884	HCT-116	colon:	n/a
50	chr7:150755834-150755884	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150755190..150756692-chr7:150922882..150924419,2	K562	blood:
2	chr7:150652621..150654850-chr7:150754233..150756879,2	MCF-7	breast:
3	chr14:20809894..20812869-chr7:150755610..150758204,2	MCF-7	breast:
4	chr7:150689613..150692426-chr7:150754513..150757333,2	MCF-7	breast:
5	chr7:150755192..150758087-chr7:150922401..150925767,3	K562	blood:

Variant related genes	Relation type
CDK5	TF binding region
SLC4A2	TF binding region
CDK5	CpG island
SLC4A2	CpG island
ENSG00000129484	Chromatin interaction
ENSG00000033050	Chromatin interaction
ENSG00000164867	Chromatin interaction
ENSG00000055118	Chromatin interaction
ENSG00000259001	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10245199	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10271154	0.84[MEX][hapmap]
rs11765015	0.80[MEX][hapmap];0.85[TSI][hapmap]
rs11773852	0.80[MEX][hapmap]
rs13247141	0.85[ASN][1000 genomes]
rs2069442	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2069443	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2069456	0.95[CEU][hapmap];0.91[MEX][hapmap];0.94[TSI][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2303929	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2303931	0.87[EUR][1000 genomes]
rs33966546	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34403003	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34812229	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs62490288	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv1022246	chr7:150619660-150779924	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv889465	chr7:150640285-150800823	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv1017863	chr7:150643928-150779924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	nsv539197	chr7:150643928-150779924	Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv1028645	chr7:150643928-150806534	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
7	nsv539198	chr7:150643928-150879259	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
8	nsv526410	chr7:150714812-150775306	Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
9	nsv889476	chr7:150729212-150951819	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	120 gene(s)	inside rSNPs	diseases
10	nsv1031733	chr7:150730999-150790517	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
11	nsv524928	chr7:150731698-150766799	Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS 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	28 gene(s)	inside rSNPs	diseases
12	nsv889477	chr7:150731698-150837529	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
13	nsv889478	chr7:150732812-150889527	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
14	nsv831188	chr7:150735204-150912875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
15	nsv889479	chr7:150736382-150785321	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription 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	45 gene(s)	inside rSNPs	diseases
16	nsv889480	chr7:150736382-150797581	Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak 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	46 gene(s)	inside rSNPs	diseases
17	nsv1028023	chr7:150738624-150790517	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
18	nsv465214	chr7:150751590-150822192	Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
19	nsv609012	chr7:150751590-150822192	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
20	nsv609013	chr7:150751590-150832913	Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1549760	GIMAP6	cis	lymphoblastoid	seeQTL
rs1549760	CYorf15B	trans	brain	seeQTL
rs1549760	KRBA1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150754000-150756600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
2	chr7:150754000-150756600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:150754200-150756400	Flanking Active TSS	Adipose Nuclei	Adipose
4	chr7:150754200-150757600	Bivalent/Poised TSS	HepG2	liver
5	chr7:150754400-150756000	Active TSS	Esophagus	oesophagus
6	chr7:150754400-150756600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr7:150754400-150757400	Active TSS	Psoas Muscle	Psoas
8	chr7:150754400-150757800	Active TSS	Aorta	Aorta
9	chr7:150754600-150756000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:150754600-150756000	Active TSS	Thymus	Thymus
11	chr7:150754600-150757400	Active TSS	Sigmoid Colon	Sigmoid Colon
12	chr7:150754600-150757600	Active TSS	Gastric	stomach
13	chr7:150754600-150757600	Active TSS	Left Ventricle	heart
14	chr7:150754600-150757600	Active TSS	Ovary	ovary
15	chr7:150754600-150758000	Active TSS	Small Intestine	intestine
16	chr7:150754800-150757400	Active TSS	Lung	lung
17	chr7:150755200-150756400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr7:150755200-150756600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:150755200-150756600	Flanking Active TSS	Fetal Muscle Trunk	muscle
20	chr7:150755200-150756600	Flanking Active TSS	HMEC	breast
21	chr7:150755200-150756600	Flanking Active TSS	NH-A	brain
22	chr7:150755400-150756200	Flanking Active TSS	Stomach Mucosa	stomach
23	chr7:150755400-150756400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
24	chr7:150755400-150756400	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr7:150755400-150756400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr7:150755400-150756400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr7:150755400-150756400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
28	chr7:150755400-150756400	Flanking Active TSS	Primary B cells from peripheral blood	blood
29	chr7:150755400-150756400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr7:150755400-150756400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
31	chr7:150755400-150756400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
32	chr7:150755400-150756400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
33	chr7:150755400-150756400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:150755400-150756400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr7:150755400-150756400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr7:150755400-150756400	Flanking Active TSS	Colon Smooth Muscle	Colon
37	chr7:150755400-150756400	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr7:150755400-150756400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
39	chr7:150755400-150756400	Flanking Active TSS	Fetal Brain Male	brain
40	chr7:150755400-150756400	Flanking Active TSS	Fetal Heart	heart
41	chr7:150755400-150756400	Flanking Active TSS	Fetal Intestine Large	intestine
42	chr7:150755400-150756400	Flanking Active TSS	Fetal Intestine Small	intestine
43	chr7:150755400-150756400	Flanking Active TSS	Fetal Thymus	thymus
44	chr7:150755400-150756400	Flanking Active TSS	Pancreas	Pancrea
45	chr7:150755400-150756400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr7:150755400-150756400	Flanking Active TSS	K562	blood
47	chr7:150755400-150756400	Flanking Active TSS	NHEK	skin
48	chr7:150755400-150756400	Flanking Active TSS	NHLF	lung
49	chr7:150755400-150756600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:150755400-150756600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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