Variant report

Variant	rs11539221
Chromosome Location	chr2:96874415-96874416
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:544)
CpG islands
(count:61)
Chromatin interactive
region (count:39)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr2:96874380-96874530	HRPEpiC	eye:	n/a	n/a
2	POLR2A	chr2:96873860-96874699	A549	lung:	n/a	n/a
3	CTCF	chr2:96874380-96874530	GM12869	blood:	n/a	n/a
4	TAF1	chr2:96873765-96874988	GM12878	blood:	n/a	n/a
5	POLR2A	chr2:96873661-96874981	HepG2	liver:	n/a	n/a
6	TAL1	chr2:96873010-96875135	K562	blood:	n/a	n/a
7	STAT5A	chr2:96874368-96874702	GM12878	blood:	n/a	n/a
8	CTCF	chr2:96874380-96874530	AG04450	lung:	n/a	n/a
9	CTCF	chr2:96874360-96874510	K562	blood:	n/a	n/a
10	NR2F2	chr2:96874377-96874852	K562	blood:	n/a	n/a
11	TAF7	chr2:96873865-96874959	H1-hESC	embryonic stem cell:	n/a	n/a
12	SIN3AK20	chr2:96873796-96874856	K562	blood:	n/a	n/a
13	POLR2A	chr2:96872978-96875681	PBDE	blood:	n/a	n/a
14	NFIC	chr2:96873871-96874935	HepG2	liver:	n/a	n/a
15	YY1	chr2:96874026-96874988	K562	blood:	n/a	chr2:96874789-96874811 chr2:96874789-96874799 chr2:96874773-96874784 chr2:96874921-96874930 chr2:96874787-96874806 chr2:96874948-96874959 chr2:96874790-96874798
16	CTCF	chr2:96874400-96874550	GM12867	blood:	n/a	n/a
17	EP300	chr2:96873724-96875048	SK-N-SH	brain:	n/a	chr2:96874809-96874825
18	SP1	chr2:96873834-96874971	A549	lung:	n/a	chr2:96874920-96874932 chr2:96874811-96874823 chr2:96874812-96874821 chr2:96874921-96874931 chr2:96874813-96874822 chr2:96874664-96874675 chr2:96874921-96874931 chr2:96874922-96874931 chr2:96874921-96874930 chr2:96874922-96874931 chr2:96874920-96874932 chr2:96874811-96874823 chr2:96874917-96874931 chr2:96874812-96874821
19	ESRRA	chr2:96873846-96874902	HepG2	liver:	n/a	n/a
20	POLR2A	chr2:96873523-96875035	GM12892	blood:	n/a	n/a
21	POLR2A	chr2:96873791-96874959	MCF-7	breast:	n/a	n/a
22	ELK1	chr2:96873129-96874895	GM12878	blood:	n/a	n/a
23	GATA3	chr2:96874333-96874986	MCF-7	breast:	n/a	n/a
24	ARID3A	chr2:96873643-96875094	HepG2	liver:	n/a	n/a
25	POLR2A	chr2:96873750-96874967	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr2:96873598-96874981	PFSK-1	brain:	n/a	n/a
27	TAF1	chr2:96873804-96875022	H1-neurons	neurons:	n/a	n/a
28	CTCF	chr2:96874380-96874530	AG04449	skin:	n/a	n/a
29	CTCF	chr2:96874400-96874550	HPAF	blood vessel:	n/a	n/a
30	GATA3	chr2:96873574-96874927	A549	lung:	n/a	n/a
31	TAF1	chr2:96873734-96874885	HepG2	liver:	n/a	n/a
32	RAD21	chr2:96873917-96874678	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr2:96873673-96875043	K562	blood:	n/a	n/a
34	MXI1	chr2:96872609-96875419	SK-N-SH	brain:	n/a	n/a
35	TBP	chr2:96873473-96874854	GM12878	blood:	n/a	n/a
36	MAFK	chr2:96874342-96874785	HepG2	liver:	n/a	n/a
37	YY1	chr2:96873745-96875027	GM12892	blood:	n/a	chr2:96874789-96874811 chr2:96874789-96874799 chr2:96874773-96874784 chr2:96874921-96874930 chr2:96874787-96874806 chr2:96874948-96874959 chr2:96874790-96874798
38	RAD21	chr2:96874365-96874516	K562	blood:	n/a	n/a
39	CTCF	chr2:96874280-96874430	HFF	foreskin:	n/a	n/a
40	NRF1	chr2:96873880-96874959	Hela-S3	cervix:	n/a	chr2:96874064-96874075 chr2:96874921-96874930
41	POLR2A	chr2:96873247-96875061	PANC-1	pancreas:	n/a	n/a
42	GTF2B	chr2:96874407-96874767	K562	blood:	n/a	n/a
43	TEAD4	chr2:96874353-96874968	K562	blood:	n/a	n/a
44	CTCF	chr2:96874399-96874548	MCF-7	breast:	n/a	n/a
45	ELF1	chr2:96873953-96874900	HepG2	liver:	n/a	n/a
46	POLR2A	chr2:96872641-96874903	HepG2	liver:	n/a	n/a
47	TAF1	chr2:96873819-96874801	GM12891	blood:	n/a	n/a
48	EGR1	chr2:96873884-96874959	HCT-116	colon:	n/a	chr2:96874919-96874929 chr2:96874916-96874929 chr2:96874921-96874931 chr2:96874664-96874678
49	CTCF	chr2:96874380-96874530	HA-sp	spinal cord:	n/a	n/a
50	ZBTB33	chr2:96874323-96874650	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96874394-96874444	SAEC	small airway:	n/a
2	chr2:96874394-96874444	HEEpiC	esophagus:	n/a
3	chr2:96874394-96874444	NH-A	brain:	n/a
4	chr2:96874394-96874444	NHBE	bronchial:	n/a
5	chr2:96874394-96874444	AG09309	skin:	n/a
6	chr2:96874394-96874444	PrEC	prostate:	n/a
7	chr2:96874394-96874444	Hela-S3	cervix:	n/a
8	chr2:96874394-96874444	T-47D	breast:	n/a
9	chr2:96874394-96874444	Hepatocyte	liver:	n/a
10	chr2:96874394-96874444	SK-N-MC	brain:	n/a
11	chr2:96874394-96874444	HIPEpiC	eye:	n/a
12	chr2:96874394-96874444	A549	lung:	n/a
13	chr2:96874394-96874444	NHDF-neo	bronchial:	n/a
14	chr2:96874394-96874444	HMEC	breast:	n/a
15	chr2:96874394-96874444	Jurkat	blood:	n/a
16	chr2:96874394-96874444	AG04449	skin:	fetal
17	chr2:96874394-96874444	HCPEpiC	choroid plexus:	n/a
18	chr2:96874394-96874444	PFSK-1	brain:	n/a
19	chr2:96874394-96874444	GM06990	blood:	n/a
20	chr2:96874394-96874444	SK-N-SH_RA	brain:	n/a
21	chr2:96874394-96874444	HCT-116	colon:	n/a
22	chr2:96874394-96874444	BJ	skin:	n/a
23	chr2:96874394-96874444	PANC-1	pancreas:	n/a
24	chr2:96874394-96874444	HRPEpiC	eye:	n/a
25	chr2:96874394-96874444	BE2_C	brain:	n/a
26	chr2:96874394-96874444	H1-hESC	embryonic stem cell:	embryo
27	chr2:96874394-96874444	HUVEC	blood vessel:	n/a
28	chr2:96874394-96874444	AG04450	lung:	fetal
29	chr2:96874394-96874444	GM12891	blood:	n/a
30	chr2:96874394-96874444	SKMC	muscle:	n/a
31	chr2:96874394-96874444	HAEpiC	amniotic membrane:	n/a
32	chr2:96874394-96874444	ProgFib	skin:	n/a
33	chr2:96874394-96874444	NB4	blood:	n/a
34	chr2:96874394-96874444	LNCaP	prostate:	n/a
35	chr2:96874394-96874444	AG10803	skin:	n/a
36	chr2:96874394-96874444	ECC-1	luminal epithelium:	n/a
37	chr2:96874394-96874444	HCF	heart:	n/a
38	chr2:96874394-96874444	ovcar-3	ovarian:	n/a
39	chr2:96874394-96874444	AG09319	gingival:	n/a
40	chr2:96874394-96874444	IMR90	lung:	fetal
41	chr2:96874394-96874444	GM12878	blood:	n/a
42	chr2:96874394-96874444	Caco-2	colon:	n/a
43	chr2:96874394-96874444	NT2-D1	testis:	n/a
44	chr2:96874394-96874444	MCF10A-Er-Src	breast:	n/a
45	chr2:96874394-96874444	U87	brain:	n/a
46	chr2:96874394-96874444	HRE	kidney:	n/a
47	chr2:96874394-96874444	HNPCEpiC	eye:	n/a
48	chr2:96874394-96874444	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:96874394-96874444	MCF-7	breast:	n/a
50	chr2:96874394-96874444	HEK293	kidney:	embryo

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:96874070..96874653-chr3:156877633..156878329,3	Hela-S3	cervix:
2	chr2:96873883..96874519-chr4:48342610..48343559,2	NB4	blood:
3	chr2:96872884..96875870-chr2:96999913..97003204,4	MCF-7	breast:
4	chr11:62609137..62610090-chr2:96874054..96874684,2	Hela-S3	cervix:
5	chr2:96873368..96875940-chr2:96925082..96928161,5	MCF-7	breast:
6	chr10:22605078..22605639-chr2:96874020..96874816,2	HCT-116	colon:
7	chr13:24734748..24735310-chr2:96874094..96874602,2	Hela-S3	cervix:
8	chr2:96874147..96874759-chr6:26033236..26033940,2	Hela-S3	cervix:
9	chr2:96873932..96874574-chr4:48271406..48272081,2	Hela-S3	cervix:
10	chr16:84537776..84538558-chr2:96873510..96874450,2	Hela-S3	cervix:
11	chr2:96872598..96876007-chr2:96924059..96928423,13	MCF-7	breast:
12	chr2:96873130..96877842-chr2:96924423..96928437,5	K562	blood:
13	chr2:96678269..96680437-chr2:96873411..96875898,2	MCF-7	breast:
14	chr2:96856180..96863246-chr2:96870668..96875373,10	MCF-7	breast:
15	chr2:96802498..96805773-chr2:96872667..96874693,3	MCF-7	breast:
16	chr2:96808076..96814305-chr2:96871431..96875215,8	MCF-7	breast:
17	chr16:54962547..54963129-chr2:96873603..96874557,2	Hela-S3	cervix:
18	chr2:96873563..96874517-chr5:90676100..90676911,2	Hela-S3	cervix:
19	chr2:96872287..96875218-chr2:97169522..97172410,2	MCF-7	breast:
20	chr1:201951655..201952284-chr2:96873670..96874594,2	HCT-116	colon:
21	chr2:58468241..58469136-chr2:96874014..96874530,2	Hela-S3	cervix:
22	chr12:7071203..7073201-chr2:96873303..96874829,2	MCF-7	breast:
23	chr2:96808739..96811929-chr2:96872960..96875920,3	MCF-7	breast:
24	chr2:96868913..96876440-chr2:96928017..96934530,23	K562	blood:
25	chr2:96870309..96876262-chr2:96928720..96933891,16	MCF-7	breast:
26	chr1:113247324..113248167-chr2:96873509..96874450,2	Hela-S3	cervix:
27	chr2:96803968..96806803-chr2:96872820..96874681,2	K562	blood:
28	chr2:96873882..96874865-chr22:41842441..41843336,2	HCT-116	colon:
29	chr2:96871739..96877156-chr2:96928674..96935050,17	K562	blood:
30	chr2:96874014..96875585-chr2:96990690..96992909,2	K562	blood:
31	chr2:96871572..96876906-chr2:96928916..96935631,15	MCF-7	breast:
32	chr2:96801466..96803641-chr2:96873708..96877456,3	MCF-7	breast:
33	chr2:96874408..96876271-chr2:96925161..96927177,2	K562	blood:
34	chr2:96873349..96876341-chr2:97001503..97003498,3	K562	blood:
35	chr2:96873776..96875796-chr2:96905403..96907728,3	MCF-7	breast:
36	chr2:96873119..96874915-chr2:97202040..97204570,2	K562	blood:
37	chr12:49658650..49659484-chr2:96874043..96874610,3	Hela-S3	cervix:
38	chr2:96872802..96875592-chr2:97201053..97203640,2	K562	blood:
39	chr17:57913629..57916404-chr2:96873395..96876100,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CIAO1-1	chr2:96874154-96874717	ENSG00000204685.5
2	lnc-CIAO1-1	chr2:96874154-96874717	NONHSAT072550

No data

Variant related genes	Relation type
STARD7	TF binding region
STARD7	CpG island
ENSG00000231584	Chromatin interaction
ENSG00000207713	Chromatin interaction
ENSG00000135605	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000176393	Chromatin interaction
ENSG00000228873	Chromatin interaction
ENSG00000158050	Chromatin interaction
ENSG00000245694	Chromatin interaction
ENSG00000148444	Chromatin interaction
ENSG00000155366	Chromatin interaction
ENSG00000115392	Chromatin interaction
ENSG00000126749	Chromatin interaction
ENSG00000140950	Chromatin interaction
ENSG00000109171	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000113369	Chromatin interaction
ENSG00000196843	Chromatin interaction
ENSG00000269897	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000204685	Chromatin interaction
ENSG00000273063	Chromatin interaction
ENSG00000198885	Chromatin interaction
ENSG00000163660	Chromatin interaction
ENSG00000167553	Chromatin interaction
ENSG00000183864	Chromatin interaction
ENSG00000135956	Chromatin interaction
ENSG00000084090	Chromatin interaction
ENSG00000182957	Chromatin interaction
ENSG00000144021	Chromatin interaction
ENSG00000121152	Chromatin interaction
ENSG00000188886	Chromatin interaction
ENSG00000163121	Chromatin interaction
ENSG00000257084	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1042361	1.00[YRI][hapmap]
rs11539223	0.88[EUR][1000 genomes]
rs17119362	0.88[EUR][1000 genomes]
rs17119627	0.84[EUR][1000 genomes]
rs17419569	0.88[EUR][1000 genomes]
rs29000576	0.84[EUR][1000 genomes]
rs55908923	0.84[EUR][1000 genomes]
rs56289221	0.88[EUR][1000 genomes]
rs67677651	0.84[EUR][1000 genomes]
rs72825836	0.84[EUR][1000 genomes]
rs72825837	0.84[EUR][1000 genomes]
rs72825845	0.84[EUR][1000 genomes]
rs72825861	0.88[EUR][1000 genomes]
rs72825869	0.88[EUR][1000 genomes]
rs72937811	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933671	chr2:96739308-97652262	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv1000780	chr2:96740430-97671395	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
3	nsv535826	chr2:96740430-97671395	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
4	nsv874677	chr2:96756547-97717345	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
5	nsv1001204	chr2:96766559-97728507	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	162 gene(s)	inside rSNPs	diseases
6	nsv535827	chr2:96766559-97728507	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
7	esv3435047	chr2:96836850-96890437	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv834305	chr2:96848898-97019476	Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription 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 target site	55 gene(s)	inside rSNPs	diseases
9	nsv874679	chr2:96860971-97184160	Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 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	chr2:96870000-96875400	Active TSS	Psoas Muscle	Psoas
2	chr2:96870400-96875400	Active TSS	Right Ventricle	heart
3	chr2:96871400-96875200	Active TSS	Left Ventricle	heart
4	chr2:96871400-96875400	Active TSS	NHLF	lung
5	chr2:96871600-96875200	Active TSS	Aorta	Aorta
6	chr2:96872200-96875000	Active TSS	GM12878-XiMat	blood
7	chr2:96872200-96875200	Active TSS	Breast Myoepithelial Primary Cells	Breast
8	chr2:96872200-96875200	Active TSS	Fetal Intestine Large	intestine
9	chr2:96872200-96875200	Active TSS	HSMMtube	muscle
10	chr2:96872600-96874600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr2:96872600-96875400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr2:96872800-96874600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
13	chr2:96872800-96875200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:96872800-96875200	Active TSS	Brain Substantia Nigra	brain
15	chr2:96872800-96875200	Active TSS	Fetal Intestine Small	intestine
16	chr2:96872800-96875200	Active TSS	Fetal Muscle Trunk	muscle
17	chr2:96872800-96875200	Active TSS	Lung	lung
18	chr2:96872800-96875200	Active TSS	Ovary	ovary
19	chr2:96873000-96874600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
20	chr2:96873000-96875000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:96873000-96875000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr2:96873000-96875000	Active TSS	Esophagus	oesophagus
23	chr2:96873000-96875200	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr2:96873000-96875200	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr2:96873000-96875200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr2:96873000-96875200	Active TSS	Pancreas	Pancrea
27	chr2:96873000-96875400	Active TSS	H1 Cell Line	embryonic stem cell
28	chr2:96873000-96875600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:96873200-96875000	Active TSS	Brain Anterior Caudate	brain
30	chr2:96873200-96875000	Active TSS	Gastric	stomach
31	chr2:96873200-96875000	Active TSS	Sigmoid Colon	Sigmoid Colon
32	chr2:96873200-96875000	Active TSS	Small Intestine	intestine
33	chr2:96873200-96875000	Active TSS	Stomach Mucosa	stomach
34	chr2:96873200-96875200	Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr2:96873200-96875200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:96873200-96875200	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr2:96873200-96875200	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr2:96873200-96875200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr2:96873200-96875200	Active TSS	Muscle Satellite Cultured Cells	--
40	chr2:96873200-96875200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr2:96873200-96875200	Active TSS	Duodenum Smooth Muscle	Duodenum
42	chr2:96873200-96875200	Active TSS	Fetal Kidney	kidney
43	chr2:96873200-96875200	Active TSS	Placenta Amnion	Placenta Amnion
44	chr2:96873200-96875400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr2:96873200-96875400	Active TSS	A549	lung
46	chr2:96873200-96875400	Active TSS	NHDF-Ad	bronchial
47	chr2:96873400-96875000	Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr2:96873400-96875000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:96873400-96875000	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr2:96873400-96875000	Active TSS	Thymus	Thymus

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