Variant report

Variant	rs187368619
Chromosome Location	chr16:70720445-70720446
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	NFIC	chr16:70720032-70720477	HepG2	liver:	n/a	n/a
2	POLR2A	chr16:70719834-70720800	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr16:70719910-70720474	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr16:70719815-70721325	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr16:70720350-70720710	H1-hESC	embryonic stem cell:	n/a	n/a
6	MXI1	chr16:70719175-70720637	HepG2	liver:	n/a	chr16:70719992-70720001
7	POLR2A	chr16:70719909-70720570	U87	brain:	n/a	n/a
8	CHD1	chr16:70718330-70720779	IMR90	lung:	n/a	n/a
9	TCF12	chr16:70719864-70720479	ECC-1	luminal epithelium:	n/a	n/a
10	MAX	chr16:70719245-70721574	NB4	blood:	n/a	chr16:70719995-70720004 chr16:70719992-70720003 chr16:70719802-70719812 chr16:70719993-70720002 chr16:70719259-70719269
11	CREB1	chr16:70718817-70720776	HepG2	liver:	n/a	n/a
12	MAX	chr16:70719282-70720824	ECC-1	luminal epithelium:	n/a	chr16:70719995-70720004 chr16:70719992-70720003 chr16:70719802-70719812 chr16:70719993-70720002
13	POLR2A	chr16:70719928-70720583	K562	blood:	n/a	n/a
14	YY1	chr16:70719805-70720469	K562	blood:	n/a	chr16:70720075-70720089 chr16:70720006-70720015
15	MAZ	chr16:70719009-70720678	K562	blood:	n/a	chr16:70719995-70720004 chr16:70719992-70720003 chr16:70719802-70719812 chr16:70719993-70720002 chr16:70719259-70719269
16	POLR2A	chr16:70719909-70720942	U87	brain:	n/a	n/a
17	POLR2A	chr16:70720266-70720506	H1-hESC	embryonic stem cell:	n/a	n/a
18	EP300	chr16:70719797-70720665	HepG2	liver:	n/a	n/a
19	TCF7L2	chr16:70719448-70720467	HCT-116	colon:	n/a	chr16:70720109-70720123
20	MAX	chr16:70714850-70722307	HepG2	liver:	n/a	chr16:70719995-70720004 chr16:70719992-70720003 chr16:70719802-70719812 chr16:70719993-70720002 chr16:70716363-70716373 chr16:70719259-70719269
21	BHLHE40	chr16:70719828-70721453	HepG2	liver:	n/a	n/a
22	BCL3	chr16:70719867-70720618	A549	lung:	n/a	chr16:70720296-70720305 chr16:70720004-70720013 chr16:70720001-70720010 chr16:70720041-70720054
23	MAX	chr16:70719354-70720614	MCF-7	breast:	n/a	chr16:70719995-70720004 chr16:70719992-70720003 chr16:70719802-70719812 chr16:70719993-70720002
24	MXI1	chr16:70718251-70721759	IMR90	lung:	n/a	chr16:70718377-70718392 chr16:70719992-70720001 chr16:70720875-70720884
25	NFIC	chr16:70719813-70720455	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr16:70718748-70721083	K562	blood:	n/a	n/a
27	POLR2A	chr16:70719721-70720471	HUVEC	blood vessel:	n/a	n/a
28	HMGN3	chr16:70719308-70720803	K562	blood:	n/a	n/a
29	REST	chr16:70718783-70720553	H1-neurons	neurons:	n/a	chr16:70719734-70719747 chr16:70720127-70720137 chr16:70718987-70719000
30	ZBTB7A	chr16:70719798-70721384	ECC-1	luminal epithelium:	n/a	chr16:70720538-70720552
31	CTCF	chr16:70720360-70720510	HBMEC	blood vessel:	n/a	n/a
32	POLR2A	chr16:70720282-70720633	PANC-1	pancreas:	n/a	n/a
33	POLR2A	chr16:70719326-70721362	K562	blood:	n/a	n/a
34	HA-E2F1	chr16:70719279-70720579	MCF-7	breast:	n/a	chr16:70719341-70719348
35	POLR2A	chr16:70720266-70720523	GM12878	blood:	n/a	n/a
36	POLR2A	chr16:70719262-70721241	HL-60	blood:	n/a	n/a
37	MXI1	chr16:70718806-70720669	SK-N-SH	brain:	n/a	chr16:70719992-70720001
38	POLR2A	chr16:70720405-70720802	GM12892	blood:	n/a	n/a
39	POLR2A	chr16:70720343-70720493	GM12878	blood:	n/a	n/a
40	EGR1	chr16:70719919-70720468	ECC-1	luminal epithelium:	n/a	chr16:70719998-70720008 chr16:70720037-70720047 chr16:70720076-70720085
41	SIN3AK20	chr16:70719003-70720472	MCF-7	breast:	n/a	n/a
42	POLR2A	chr16:70707751-70721480	HepG2	liver:	n/a	n/a
43	MAZ	chr16:70717552-70721715	IMR90	lung:	n/a	chr16:70719995-70720004 chr16:70719992-70720003 chr16:70719802-70719812 chr16:70719993-70720002 chr16:70719259-70719269
44	CTCF	chr16:70720380-70720530	Caco-2	colon:	n/a	n/a
45	ZBTB7A	chr16:70719806-70720961	ECC-1	luminal epithelium:	n/a	chr16:70720538-70720552
46	POLR2A	chr16:70719904-70720535	HUVEC	blood vessel:	n/a	n/a
47	HDAC2	chr16:70719829-70720543	HepG2	liver:	n/a	chr16:70720075-70720084
48	POLR2A	chr16:70719548-70720622	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr16:70719356-70720727	NB4	blood:	n/a	n/a
50	POLR2A	chr16:70718864-70721688	HL-60	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70720440-70720490	GM06990	blood:	n/a
2	chr16:70720440-70720490	HEK293	kidney:	embryo
3	chr16:70720440-70720490	Caco-2	colon:	n/a
4	chr16:70720440-70720490	HRE	kidney:	n/a
5	chr16:70720440-70720490	A549	lung:	n/a
6	chr16:70720440-70720490	NHDF-neo	bronchial:	n/a
7	chr16:70720440-70720490	AG10803	skin:	n/a
8	chr16:70720440-70720490	NHBE	bronchial:	n/a
9	chr16:70720440-70720490	Hepatocyte	liver:	n/a
10	chr16:70720440-70720490	PFSK-1	brain:	n/a
11	chr16:70720440-70720490	GM12892	blood:	n/a
12	chr16:70720440-70720490	SK-N-SH_RA	brain:	n/a
13	chr16:70720440-70720490	HUVEC	blood vessel:	n/a
14	chr16:70720440-70720490	BE2_C	brain:	n/a
15	chr16:70720440-70720490	IMR90	lung:	fetal
16	chr16:70720440-70720490	HCM	heart:	n/a
17	chr16:70720440-70720490	SK-N-SH	brain:	n/a
18	chr16:70720440-70720490	NB4	blood:	n/a
19	chr16:70720440-70720490	LNCaP	prostate:	n/a
20	chr16:70720440-70720490	MCF-7	breast:	n/a
21	chr16:70720440-70720490	BJ	skin:	n/a
22	chr16:70720440-70720490	HNPCEpiC	eye:	n/a
23	chr16:70720440-70720490	NT2-D1	testis:	n/a
24	chr16:70720440-70720490	GM12878	blood:	n/a
25	chr16:70720440-70720490	AG04450	lung:	fetal
26	chr16:70720440-70720490	SKMC	muscle:	n/a
27	chr16:70720440-70720490	U87	brain:	n/a
28	chr16:70720440-70720490	ECC-1	luminal epithelium:	n/a
29	chr16:70720440-70720490	NH-A	brain:	n/a
30	chr16:70720440-70720490	HRPEpiC	eye:	n/a
31	chr16:70720440-70720490	GM19239	blood:	n/a
32	chr16:70720440-70720490	MCF10A-Er-Src	breast:	n/a
33	chr16:70720440-70720490	HPAEpiC	pulmonary alveolar:	n/a
34	chr16:70720440-70720490	HCPEpiC	choroid plexus:	n/a
35	chr16:70720440-70720490	H1-hESC	embryonic stem cell:	embryo
36	chr16:70720440-70720490	AG09309	skin:	n/a
37	chr16:70720440-70720490	SAEC	small airway:	n/a
38	chr16:70720440-70720490	T-47D	breast:	n/a
39	chr16:70720440-70720490	ProgFib	skin:	n/a
40	chr16:70720440-70720490	HEEpiC	esophagus:	n/a
41	chr16:70720440-70720490	CMK	blood:	n/a
42	chr16:70720440-70720490	HL-60	blood:	n/a
43	chr16:70720440-70720490	GM12891	blood:	n/a
44	chr16:70720440-70720490	HRCEpiC	kidney:	n/a
45	chr16:70720440-70720490	RPTEC	kidney:	n/a
46	chr16:70720440-70720490	HCT-116	colon:	n/a
47	chr16:70720440-70720490	Hela-S3	cervix:	n/a
48	chr16:70720440-70720490	PANC-1	pancreas:	n/a
49	chr16:70720440-70720490	HCF	heart:	n/a
50	chr16:70720440-70720490	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:70699407..70701314-chr16:70720329..70722044,2	MCF-7	breast:
2	chr16:70709373..70712593-chr16:70717107..70721470,4	MCF-7	breast:
3	chr16:70716857..70722605-chr16:70776377..70783146,15	MCF-7	breast:
4	chr16:70555634..70562342-chr16:70718026..70723686,6	MCF-7	breast:
5	chr1:28974074..28976735-chr16:70718527..70720954,2	K562	blood:
6	chr16:70715424..70721545-chr16:70778213..70783786,16	MCF-7	breast:
7	chr16:70716977..70720923-chr16:70779925..70783515,4	K562	blood:

Variant related genes	Relation type
MTSS1L	TF binding region
MTSS1L	CpG island
ENSG00000270103	Chromatin interaction
ENSG00000103043	Chromatin interaction
ENSG00000132613	Chromatin interaction
ENSG00000260156	Chromatin interaction
ENSG00000103051	Chromatin interaction
ENSG00000189091	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517391	chr16:70666410-70840490	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv457517	chr16:70666722-70840490	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' 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
3	nsv572945	chr16:70666722-70840490	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv906874	chr16:70677785-70740707	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv906875	chr16:70677785-70742536	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv906876	chr16:70677785-70757555	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer 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 miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv906877	chr16:70677785-70766378	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv906878	chr16:70677785-70782922	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS 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	19 gene(s)	inside rSNPs	diseases
9	nsv906879	chr16:70677785-70790831	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS 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	19 gene(s)	inside rSNPs	diseases
10	nsv906880	chr16:70677785-70796515	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv906882	chr16:70690989-70725815	Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
12	nsv572946	chr16:70694000-70740707	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
13	nsv471094	chr16:70694000-70749970	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
14	nsv906884	chr16:70696009-70725815	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
15	nsv906885	chr16:70696367-70742536	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
16	nsv1059226	chr16:70708698-70779144	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
17	nsv906886	chr16:70712549-70727324	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
18	nsv906887	chr16:70714434-70727324	Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
19	nsv572947	chr16:70714434-70731870	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
20	nsv906888	chr16:70716742-70742536	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS 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	12 gene(s)	inside rSNPs	diseases
21	esv3400505	chr16:70718476-70721024	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
22	esv3372973	chr16:70718876-70721424	Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70717800-70720600	Active TSS	Aorta	Aorta
2	chr16:70718600-70720600	Flanking Active TSS	Primary hematopoietic stem cells	blood
3	chr16:70718600-70720800	Active TSS	H9 Cell Line	embryonic stem cell
4	chr16:70719000-70720600	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr16:70719000-70720600	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr16:70719400-70720600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
7	chr16:70719400-70727800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr16:70719400-70729200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr16:70719400-70729400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr16:70719800-70732400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr16:70720000-70720600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr16:70720000-70720600	Flanking Active TSS	NHEK	skin
13	chr16:70720000-70720800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr16:70720000-70721000	Enhancers	Small Intestine	intestine
15	chr16:70720000-70721200	Enhancers	Stomach Mucosa	stomach
16	chr16:70720000-70721400	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr16:70720000-70732200	Enhancers	Fetal Brain Male	brain
18	chr16:70720200-70720600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr16:70720200-70720600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr16:70720200-70720600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr16:70720200-70720600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr16:70720200-70720600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr16:70720200-70720600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr16:70720200-70720600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr16:70720200-70720600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
26	chr16:70720200-70720600	Flanking Active TSS	Fetal Intestine Large	intestine
27	chr16:70720200-70720600	Flanking Active TSS	Fetal Lung	lung
28	chr16:70720200-70720600	Flanking Active TSS	Placenta	Placenta
29	chr16:70720200-70720600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
30	chr16:70720200-70720600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
31	chr16:70720200-70720600	Flanking Active TSS	HUVEC	blood vessel
32	chr16:70720200-70720600	Flanking Active TSS	NH-A	brain
33	chr16:70720200-70720600	Flanking Active TSS	Osteobl	bone
34	chr16:70720200-70720800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr16:70720200-70720800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr16:70720200-70720800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr16:70720200-70720800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr16:70720200-70720800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr16:70720200-70720800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr16:70720200-70720800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
41	chr16:70720200-70720800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr16:70720200-70720800	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr16:70720200-70720800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
44	chr16:70720200-70720800	Flanking Active TSS	Brain Substantia Nigra	brain
45	chr16:70720200-70720800	Flanking Active TSS	Thymus	Thymus
46	chr16:70720200-70720800	Flanking Active TSS	Dnd41	blood
47	chr16:70720200-70720800	Flanking Active TSS	Hela-S3	cervix
48	chr16:70720200-70721000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr16:70720200-70721000	Flanking Active TSS	Fetal Muscle Trunk	muscle
50	chr16:70720200-70721000	Flanking Active TSS	NHLF	lung

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