Variant report

Variant	rs74015088
Chromosome Location	chr16:31190929-31190930
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	RCOR1	chr16:31189939-31192131	GM12878	blood:	n/a	n/a
2	ELF1	chr16:31190795-31192249	MCF-7	breast:	n/a	chr16:31191571-31191580 chr16:31191382-31191393 chr16:31191871-31191883
3	YY1	chr16:31190671-31191205	GM12891	blood:	n/a	chr16:31191138-31191149 chr16:31191166-31191175
4	GTF2F1	chr16:31190901-31192119	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD1	chr16:31190257-31193157	GM12878	blood:	n/a	chr16:31191164-31191174 chr16:31192004-31192013 chr16:31191558-31191568 chr16:31191159-31191169
6	ZKSCAN1	chr16:31190679-31192072	Hela-S3	cervix:	n/a	n/a
7	GTF2F1	chr16:31190885-31191915	Hela-S3	cervix:	n/a	n/a
8	MAX	chr16:31190500-31192802	HepG2	liver:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
9	MAFK	chr16:31190899-31192103	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr16:31190828-31192314	SK-N-MC	brain:	n/a	n/a
11	TAF1	chr16:31190818-31192243	MCF-7	breast:	n/a	n/a
12	ZNF143	chr16:31190717-31192018	K562	blood:	n/a	chr16:31191864-31191882
13	TBP	chr16:31190103-31192399	H1-hESC	embryonic stem cell:	n/a	n/a
14	RELA	chr16:31190259-31192150	GM12892	blood:	n/a	n/a
15	RCOR1	chr16:31190619-31192193	Hela-S3	cervix:	n/a	n/a
16	ZNF143	chr16:31190554-31191667	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr16:31190873-31192306	GM12878	blood:	n/a	chr16:31191164-31191174 chr16:31192004-31192013 chr16:31191558-31191568 chr16:31191159-31191169
18	GTF2F1	chr16:31190923-31192232	K562	blood:	n/a	n/a
19	POLR2A	chr16:31190336-31191198	GM12891	blood:	n/a	n/a
20	JUND	chr16:31190149-31192543	GM12878	blood:	n/a	chr16:31191742-31191751
21	MTA3	chr16:31189905-31192315	GM12878	blood:	n/a	n/a
22	MAX	chr16:31190581-31193182	A549	lung:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
23	MYC	chr16:31190763-31192415	A549	lung:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
24	POLR2A	chr16:31190856-31192293	HEK293	kidney:	n/a	n/a
25	POLR2A	chr16:31190666-31192976	Hela-S3	cervix:	n/a	n/a
26	STAT5A	chr16:31190839-31192101	GM12878	blood:	n/a	chr16:31191366-31191374
27	HEY1	chr16:31190841-31193110	K562	blood:	n/a	chr16:31191879-31191894 chr16:31191563-31191578 chr16:31191399-31191414 chr16:31191657-31191672 chr16:31191575-31191590
28	POLR2A	chr16:31190895-31193319	K562	blood:	n/a	n/a
29	POLR2A	chr16:31190754-31192802	Hela-S3	cervix:	n/a	n/a
30	HMGN3	chr16:31190738-31192265	K562	blood:	n/a	n/a
31	SIN3AK20	chr16:31190767-31192780	PANC-1	pancreas:	n/a	n/a
32	E2F4	chr16:31190904-31192678	K562	blood:	n/a	chr16:31191743-31191755 chr16:31191735-31191747 chr16:31191653-31191664 chr16:31191653-31191660 chr16:31192218-31192230 chr16:31191663-31191675 chr16:31191650-31191667 chr16:31191448-31191457 chr16:31192219-31192226 chr16:31191652-31191661 chr16:31191400-31191409 chr16:31191142-31191152 chr16:31192094-31192105 chr16:31192219-31192226 chr16:31191166-31191175 chr16:31192218-31192227 chr16:31192165-31192172 chr16:31192219-31192226 chr16:31191929-31191938 chr16:31191653-31191664 chr16:31191653-31191664 chr16:31192031-31192040
33	TAF1	chr16:31190735-31192169	H1-neurons	neurons:	n/a	n/a
34	CHD1	chr16:31190198-31193440	IMR90	lung:	n/a	chr16:31191164-31191174 chr16:31192004-31192013 chr16:31191558-31191568 chr16:31191159-31191169
35	RUNX3	chr16:31190207-31192328	GM12878	blood:	n/a	n/a
36	POLR2A	chr16:31190807-31192356	MCF-7	breast:	n/a	n/a
37	POLR2A	chr16:31190841-31192248	PBDE	blood:	n/a	n/a
38	TAF1	chr16:31190766-31192283	ECC-1	luminal epithelium:	n/a	n/a
39	POLR2A	chr16:31190795-31192255	HCT-116	colon:	n/a	n/a
40	POLR2A	chr16:31190906-31193251	K562	blood:	n/a	n/a
41	MAX	chr16:31190460-31192399	HCT-116	colon:	n/a	chr16:31192111-31192120 chr16:31190763-31190772
42	TBL1XR1	chr16:31190182-31192284	GM12878	blood:	n/a	n/a
43	TAF1	chr16:31190826-31192173	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr16:31190731-31193336	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr16:31190660-31197223	SK-N-MC	brain:	n/a	n/a
46	YY1	chr16:31190882-31192252	K562	blood:	n/a	chr16:31191138-31191149 chr16:31191574-31191588 chr16:31192116-31192127 chr16:31191710-31191718 chr16:31191571-31191580 chr16:31191565-31191579 chr16:31191707-31191729 chr16:31191707-31191717 chr16:31192119-31192133 chr16:31191857-31191868 chr16:31191706-31191718 chr16:31191166-31191175
47	CREB1	chr16:31190696-31192214	H1-hESC	embryonic stem cell:	n/a	n/a
48	SP1	chr16:31190846-31192317	K562	blood:	n/a	chr16:31191029-31191043 chr16:31191977-31191986 chr16:31191165-31191175 chr16:31191947-31191956 chr16:31192118-31192132 chr16:31192121-31192133 chr16:31191447-31191459 chr16:31191945-31191957 chr16:31191166-31191175 chr16:31191448-31191457 chr16:31191352-31191362 chr16:31191055-31191069 chr16:31191165-31191179 chr16:31192121-31192133 chr16:31191946-31191956 chr16:31191447-31191459 chr16:31191351-31191363 chr16:31191165-31191174 chr16:31191164-31191176 chr16:31191165-31191175 chr16:31191351-31191363 chr16:31191946-31191955 chr16:31191449-31191458 chr16:31191165-31191174 chr16:31192122-31192131 chr16:31191945-31191957 chr16:31191164-31191176 chr16:31191444-31191458 chr16:31191946-31191960 chr16:31191348-31191362 chr16:31191352-31191361
49	SMC3	chr16:31190735-31192094	Hela-S3	cervix:	n/a	chr16:31191445-31191455 chr16:31191168-31191178
50	ATF2	chr16:31190741-31192311	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:31126778..31130864-chr16:31189092..31195209,17	K562	blood:
2	chr16:31172186..31178618-chr16:31189730..31194059,7	MCF-7	breast:
3	chr16:31189605..31193047-chr16:31225207..31229243,8	MCF-7	breast:
4	chr16:31127491..31131830-chr16:31190393..31192870,6	MCF-7	breast:
5	chr13:49549672..49551500-chr16:31190171..31192875,2	MCF-7	breast:
6	chr10:60144727..60145603-chr16:31190797..31191683,3	Hela-S3	cervix:
7	chr16:31190068..31192732-chr16:31364834..31366748,2	MCF-7	breast:
8	chr16:31190494..31194030-chr16:31469173..31472392,6	MCF-7	breast:
9	chr16:31098939..31101568-chr16:31190288..31192839,3	MCF-7	breast:
10	chr16:31190876..31193496-chr16:31467915..31469543,2	K562	blood:
11	chr16:31189986..31193003-chr16:31453112..31456004,3	MCF-7	breast:
12	chr16:31118660..31120523-chr16:31190662..31192940,2	MCF-7	breast:
13	chr16:31082536..31087626-chr16:31189682..31193300,10	K562	blood:
14	chr16:31104719..31108663-chr16:31190189..31193568,7	MCF-7	breast:
15	chr16:31103018..31109714-chr16:31190079..31193155,12	K562	blood:
16	chr16:31146560..31148604-chr16:31190124..31192018,2	K562	blood:
17	chr16:31190869..31192823-chr20:49543884..49546240,2	MCF-7	breast:
18	chr16:30958732..30963097-chr16:31189619..31195213,8	K562	blood:
19	chr16:30708214..30710330-chr16:31190333..31193156,2	K562	blood:
20	chr16:31140279..31143875-chr16:31189793..31193230,5	MCF-7	breast:
21	chr16:31190054..31194646-chr16:31224217..31229118,11	MCF-7	breast:
22	chr16:30933224..30936181-chr16:31190353..31192929,3	MCF-7	breast:
23	chr16:31117735..31121210-chr16:31190065..31193528,11	K562	blood:
24	chr16:31149707..31163529-chr16:31187237..31198825,44	K562	blood:
25	chr16:31151687..31162079-chr16:31189046..31201898,43	K562	blood:
26	chr16:31189995..31193017-chr16:31468555..31472249,11	K562	blood:
27	chr16:31190260..31192807-chr6:26031049..26033016,2	K562	blood:
28	chr16:31007263..31009136-chr16:31190228..31192701,2	MCF-7	breast:
29	chr16:30967386..30971624-chr16:31189375..31193961,9	K562	blood:
30	chr16:30994008..30999750-chr16:31190407..31194686,5	K562	blood:
31	chr16:30967331..30971455-chr16:31189672..31193521,14	K562	blood:
32	chr16:31139340..31148115-chr16:31189133..31193213,16	MCF-7	breast:
33	chr16:31103889..31108377-chr16:31189247..31192858,8	MCF-7	breast:
34	chr16:31103018..31108579-chr16:31189579..31192896,9	K562	blood:
35	chr16:31082583..31087626-chr16:31190328..31193369,8	K562	blood:
36	chr16:31189717..31191990-chr6:151711401..151713605,2	K562	blood:
37	chr16:30935927..30937493-chr16:31190517..31192070,2	K562	blood:
38	chr16:31149322..31163059-chr16:31188531..31198512,46	MCF-7	breast:
39	chr16:30952173..30954212-chr16:31190131..31192878,2	MCF-7	breast:
40	chr16:31152041..31157483-chr16:31189137..31194314,15	MCF-7	breast:
41	chr16:31006037..31010198-chr16:31189951..31194376,15	K562	blood:
42	chr16:31190412..31192791-chr16:31452849..31455958,6	MCF-7	breast:
43	chr16:31144485..31148429-chr16:31189146..31193121,7	MCF-7	breast:
44	chr16:31190765..31191398-chr9:140172167..140172759,2	Hela-S3	cervix:
45	chr10:8099490..8102473-chr16:31190393..31192095,2	MCF-7	breast:
46	chr16:31190736..31191506-chr7:107384185..107384693,2	Hela-S3	cervix:
47	chr16:31043530..31046862-chr16:31190161..31192908,5	K562	blood:
48	chr16:31190647..31191297-chr2:179315444..179315986,2	Hela-S3	cervix:
49	chr16:31190898..31191887-chrX:153714080..153715002,2	Hela-S3	cervix:
50	chr16:31126872..31130668-chr16:31190197..31195425,8	MCF-7	breast:

Variant related genes	Relation type
FUS	TF binding region
ENSG00000263343	Chromatin interaction
ENSG00000180228	Chromatin interaction
ENSG00000052344	Chromatin interaction
ENSG00000261487	Chromatin interaction
ENSG00000099364	Chromatin interaction
ENSG00000181472	Chromatin interaction
ENSG00000178226	Chromatin interaction
ENSG00000099377	Chromatin interaction
ENSG00000099365	Chromatin interaction
ENSG00000260911	Chromatin interaction
ENSG00000260852	Chromatin interaction
ENSG00000080603	Chromatin interaction
ENSG00000261385	Chromatin interaction
ENSG00000255439	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000175938	Chromatin interaction
ENSG00000261840	Chromatin interaction
ENSG00000241764	Chromatin interaction
ENSG00000102178	Chromatin interaction
ENSG00000262766	Chromatin interaction
ENSG00000105879	Chromatin interaction
ENSG00000167395	Chromatin interaction
ENSG00000102531	Chromatin interaction
ENSG00000177238	Chromatin interaction
ENSG00000103510	Chromatin interaction
ENSG00000101126	Chromatin interaction
ENSG00000107485	Chromatin interaction
ENSG00000268863	Chromatin interaction
ENSG00000167394	Chromatin interaction
ENSG00000252809	Chromatin interaction
ENSG00000151006	Chromatin interaction
ENSG00000261474	Chromatin interaction
ENSG00000169896	Chromatin interaction
ENSG00000198113	Chromatin interaction
ENSG00000169900	Chromatin interaction
ENSG00000261124	Chromatin interaction
ENSG00000176723	Chromatin interaction
ENSG00000029363	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000103496	Chromatin interaction
ENSG00000120915	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000167397	Chromatin interaction
ENSG00000108064	Chromatin interaction
ENSG00000140678	Chromatin interaction
ENSG00000124693	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs41371846	1.00[AMR][1000 genomes]
rs41520646	1.00[AMR][1000 genomes]
rs56751167	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57483806	1.00[AMR][1000 genomes]
rs58114676	1.00[AMR][1000 genomes]
rs61417139	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015052	1.00[AMR][1000 genomes]
rs74015064	1.00[AMR][1000 genomes]
rs74015067	1.00[AMR][1000 genomes]
rs74015073	1.00[AMR][1000 genomes]
rs74015098	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74015100	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers 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 miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
10	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
11	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases
12	nsv542900	chr16:31137352-31197027	Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	165 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	chr16:31189800-31191000	Flanking Active TSS	GM12878-XiMat	blood
2	chr16:31190000-31191000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr16:31190000-31191000	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr16:31190000-31191000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr16:31190000-31191000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr16:31190000-31191000	Flanking Active TSS	Dnd41	blood
7	chr16:31190000-31191000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr16:31190000-31191200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr16:31190000-31193600	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr16:31190000-31193600	Active TSS	H9 Cell Line	embryonic stem cell
11	chr16:31190200-31191000	Flanking Active TSS	Primary B cells from peripheral blood	blood
12	chr16:31190200-31191000	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr16:31190200-31191000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
14	chr16:31190200-31191000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr16:31190200-31191000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr16:31190200-31191000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr16:31190200-31191000	Flanking Active TSS	Adipose Nuclei	Adipose
18	chr16:31190200-31191000	Flanking Active TSS	Stomach Smooth Muscle	stomach
19	chr16:31190200-31192200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr16:31190200-31192600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr16:31190200-31192600	Active TSS	NHLF	lung
22	chr16:31190200-31193000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr16:31190200-31193800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr16:31190200-31193800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr16:31190400-31191000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
26	chr16:31190400-31191000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
27	chr16:31190400-31191000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr16:31190400-31191000	Flanking Active TSS	Liver	Liver
29	chr16:31190400-31191000	Flanking Active TSS	Duodenum Mucosa	Duodenum
30	chr16:31190400-31191000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
31	chr16:31190400-31191000	Flanking Active TSS	Fetal Muscle Leg	muscle
32	chr16:31190400-31191000	Flanking Active TSS	Placenta	Placenta
33	chr16:31190400-31191000	Flanking Active TSS	Fetal Thymus	thymus
34	chr16:31190400-31191000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr16:31190400-31191000	Flanking Active TSS	HUVEC	blood vessel
36	chr16:31190400-31191000	Flanking Active TSS	NH-A	brain
37	chr16:31190400-31191400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr16:31190400-31192200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr16:31190400-31192200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
40	chr16:31190400-31192200	Active TSS	Colonic Mucosa	Colon
41	chr16:31190400-31192400	Active TSS	Fetal Intestine Small	intestine
42	chr16:31190400-31192600	Active TSS	Fetal Muscle Trunk	muscle
43	chr16:31190400-31192600	Active TSS	Right Ventricle	heart
44	chr16:31190400-31192800	Active TSS	Fetal Lung	lung
45	chr16:31190400-31193000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr16:31190400-31193400	Active TSS	Psoas Muscle	Psoas
47	chr16:31190400-31193600	Active TSS	Pancreatic Islets	Pancreatic Islet
48	chr16:31190400-31193600	Active TSS	Left Ventricle	heart
49	chr16:31190600-31191000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
50	chr16:31190600-31191000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast

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