Variant report

Variant	rs571328605
Chromosome Location	chr2:97481982-97481983
allele	C/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	TCF3	chr2:97481888-97482708	GM12878	blood:	n/a	n/a
2	POLR2A	chr2:97481916-97482212	HUVEC	blood vessel:	n/a	n/a
3	EGR1	chr2:97481597-97482456	K562	blood:	n/a	chr2:97481897-97481910 chr2:97482282-97482296 chr2:97481898-97481907 chr2:97481896-97481910 chr2:97481896-97481911 chr2:97481897-97481910 chr2:97481902-97481912 chr2:97481894-97481908 chr2:97482256-97482270 chr2:97481897-97481907 chr2:97481897-97481910 chr2:97481897-97481910
4	BRCA1	chr2:97481977-97482143	H1-hESC	embryonic stem cell:	n/a	n/a
5	NR3C1	chr2:97481553-97482675	A549	lung:	n/a	n/a
6	CTCF	chr2:97481880-97482030	GM12878	blood:	n/a	n/a
7	CTCF	chr2:97481900-97482050	HRPEpiC	eye:	n/a	n/a
8	POLR2A	chr2:97481096-97483863	GM12878	blood:	n/a	n/a
9	CTCF	chr2:97481980-97482130	RPTEC	kidney:	n/a	n/a
10	SP2	chr2:97481721-97482153	H1-hESC	embryonic stem cell:	n/a	chr2:97481913-97481923
11	POLR2A	chr2:97481902-97482129	H1-hESC	embryonic stem cell:	n/a	n/a
12	TAF1	chr2:97481915-97482058	PFSK-1	brain:	n/a	n/a
13	FOS	chr2:97481759-97482116	K562	blood:	n/a	n/a
14	CTCF	chr2:97481896-97482071	LNCaP	prostate:	n/a	n/a
15	CTCF	chr2:97481900-97482050	HCT-116	colon:	n/a	n/a
16	CTCF	chr2:97481904-97482112	NHEK	skin:	n/a	n/a
17	MAX	chr2:97481268-97482615	ECC-1	luminal epithelium:	n/a	chr2:97481548-97481558 chr2:97481901-97481911
18	CTCF	chr2:97481920-97482070	HBMEC	blood vessel:	n/a	n/a
19	SP1	chr2:97481753-97482048	K562	blood:	n/a	chr2:97481896-97481905 chr2:97481901-97481910 chr2:97481902-97481911 chr2:97481900-97481912 chr2:97481895-97481904 chr2:97481904-97481925 chr2:97481901-97481915 chr2:97481901-97481911 chr2:97481900-97481912 chr2:97481894-97481906 chr2:97481894-97481906
20	CBX3	chr2:97481792-97482205	K562	blood:	n/a	n/a
21	SP1	chr2:97481624-97482367	A549	lung:	n/a	chr2:97481896-97481905 chr2:97481901-97481910 chr2:97481902-97481911 chr2:97481900-97481912 chr2:97481895-97481904 chr2:97481904-97481925 chr2:97481901-97481915 chr2:97481901-97481911 chr2:97481900-97481912 chr2:97481894-97481906 chr2:97481894-97481906
22	NFYA	chr2:97481748-97482188	K562	blood:	n/a	chr2:97481907-97481925 chr2:97481946-97481958 chr2:97481911-97481926 chr2:97481911-97481926
23	TAF1	chr2:97481800-97482206	SK-N-SH	brain:	n/a	n/a
24	SIN3AK20	chr2:97481051-97482332	MCF-7	breast:	n/a	n/a
25	TCF12	chr2:97481604-97482660	ECC-1	luminal epithelium:	n/a	chr2:97482002-97482012
26	ZNF263	chr2:97481138-97486512	HEK293-T-REx	kidney:	n/a	chr2:97486292-97486301 chr2:97484433-97484454
27	MAX	chr2:97481365-97482191	SK-N-SH	brain:	n/a	chr2:97481548-97481558 chr2:97481901-97481911
28	CTCF	chr2:97481831-97482440	K562	blood:	n/a	n/a
29	CTCF	chr2:97481900-97482050	A549	lung:	n/a	n/a
30	CTCF	chr2:97481888-97482126	MCF-7	breast:	n/a	n/a
31	NFIC	chr2:97481854-97482369	HepG2	liver:	n/a	n/a
32	CTCF	chr2:97481901-97482097	GM12878	blood:	n/a	n/a
33	TAF1	chr2:97481420-97482661	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr2:97481917-97482096	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:97481860-97482010	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr2:97481088-97483359	Hela-S3	cervix:	n/a	n/a
37	PML	chr2:97481662-97482490	MCF-7	breast:	n/a	n/a
38	CREB1	chr2:97481499-97482739	A549	lung:	n/a	n/a
39	POLR2A	chr2:97481498-97482738	HUVEC	blood vessel:	n/a	n/a
40	SP1	chr2:97481736-97482228	H1-hESC	embryonic stem cell:	n/a	chr2:97481896-97481905 chr2:97481901-97481910 chr2:97481902-97481911 chr2:97481900-97481912 chr2:97481895-97481904 chr2:97481904-97481925 chr2:97481901-97481915 chr2:97481901-97481911 chr2:97481900-97481912 chr2:97481894-97481906 chr2:97481894-97481906
41	RCOR1	chr2:97481636-97482383	GM12878	blood:	n/a	n/a
42	EGR1	chr2:97481692-97482221	ECC-1	luminal epithelium:	n/a	chr2:97481897-97481910 chr2:97481898-97481907 chr2:97481896-97481910 chr2:97481896-97481911 chr2:97481897-97481910 chr2:97481902-97481912 chr2:97481894-97481908 chr2:97481897-97481907 chr2:97481897-97481910 chr2:97481897-97481910
43	CTCF	chr2:97481920-97482070	GM12865	blood:	n/a	n/a
44	POLR2A	chr2:97481236-97482891	GM15510	blood:	n/a	n/a
45	YY1	chr2:97481692-97482414	ECC-1	luminal epithelium:	n/a	chr2:97481751-97481760 chr2:97481899-97481908 chr2:97481708-97481722 chr2:97481900-97481914
46	POLR2A	chr2:97481531-97482767	HEK293	kidney:	n/a	n/a
47	MAX	chr2:97481293-97483422	A549	lung:	n/a	chr2:97481548-97481558 chr2:97481901-97481911
48	MXI1	chr2:97481116-97482966	GM12878	blood:	n/a	n/a
49	CTCF	chr2:97481705-97482787	IMR90	lung:	n/a	n/a
50	CTCF	chr2:97481860-97482010	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:97481963-97482013	U87	brain:	n/a
2	chr2:97481963-97482013	LNCaP	prostate:	n/a
3	chr2:97481963-97482013	PFSK-1	brain:	n/a
4	chr2:97481963-97482013	ovcar-3	ovarian:	n/a
5	chr2:97481963-97482013	RPTEC	kidney:	n/a
6	chr2:97481963-97482013	HL-60	blood:	n/a
7	chr2:97481963-97482013	MCF-7	breast:	n/a
8	chr2:97481963-97482013	AG10803	skin:	n/a
9	chr2:97481963-97482013	HAEpiC	amniotic membrane:	n/a
10	chr2:97481963-97482013	HRE	kidney:	n/a
11	chr2:97481963-97482013	SK-N-SH_RA	brain:	n/a
12	chr2:97481963-97482013	GM12891	blood:	n/a
13	chr2:97481963-97482013	SAEC	small airway:	n/a
14	chr2:97481963-97482013	BE2_C	brain:	n/a
15	chr2:97481963-97482013	K562	blood:	n/a
16	chr2:97481963-97482013	SK-N-SH	brain:	n/a
17	chr2:97481963-97482013	NH-A	brain:	n/a
18	chr2:97481963-97482013	NHBE	bronchial:	n/a
19	chr2:97481963-97482013	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:97481963-97482013	GM06990	blood:	n/a
21	chr2:97481963-97482013	ECC-1	luminal epithelium:	n/a
22	chr2:97481963-97482013	Hepatocyte	liver:	n/a
23	chr2:97481963-97482013	HRPEpiC	eye:	n/a
24	chr2:97481963-97482013	NHDF-neo	bronchial:	n/a
25	chr2:97481963-97482013	HCF	heart:	n/a
26	chr2:97481963-97482013	Hela-S3	cervix:	n/a
27	chr2:97481963-97482013	AG04449	skin:	fetal
28	chr2:97481963-97482013	HEEpiC	esophagus:	n/a
29	chr2:97481963-97482013	PrEC	prostate:	n/a
30	chr2:97481963-97482013	SKMC	muscle:	n/a
31	chr2:97481963-97482013	Jurkat	blood:	n/a
32	chr2:97481963-97482013	GM12892	blood:	n/a
33	chr2:97481963-97482013	CMK	blood:	n/a
34	chr2:97481963-97482013	AG09319	gingival:	n/a
35	chr2:97481963-97482013	HNPCEpiC	eye:	n/a
36	chr2:97481963-97482013	HEK293	kidney:	embryo
37	chr2:97481963-97482013	HIPEpiC	eye:	n/a
38	chr2:97481963-97482013	HRCEpiC	kidney:	n/a
39	chr2:97481963-97482013	Caco-2	colon:	n/a
40	chr2:97481963-97482013	HCM	heart:	n/a
41	chr2:97481963-97482013	A549	lung:	n/a
42	chr2:97481963-97482013	HepG2	liver:	n/a
43	chr2:97481963-97482013	PANC-1	pancreas:	n/a
44	chr2:97481963-97482013	T-47D	breast:	n/a
45	chr2:97481963-97482013	NT2-D1	testis:	n/a
46	chr2:97481963-97482013	HCPEpiC	choroid plexus:	n/a
47	chr2:97481963-97482013	NB4	blood:	n/a
48	chr2:97481963-97482013	GM19239	blood:	n/a
49	chr2:97481963-97482013	HUVEC	blood vessel:	n/a
50	chr2:97481963-97482013	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:97481962..97482603-chr3:195163221..195164183,2	Hela-S3	cervix:
2	chr2:97302043..97304772-chr2:97480834..97485283,4	K562	blood:
3	chr2:97481720..97483625-chr2:97563695..97565331,2	MCF-7	breast:
4	chr2:97302952..97305022-chr2:97481063..97483448,2	MCF-7	breast:
5	chr2:97481636..97484312-chr2:97528160..97530681,3	MCF-7	breast:
6	chr2:97481114..97483138-chr2:97559703..97563563,4	MCF-7	breast:
7	chr2:97481648..97486150-chr2:97531417..97538119,10	MCF-7	breast:
8	chr2:97303859..97305572-chr2:97481972..97484956,2	K562	blood:
9	chr2:97480973..97483903-chr2:97621623..97628750,6	MCF-7	breast:
10	chr2:97480158..97482561-chr2:97778545..97780856,2	MCF-7	breast:
11	chr1:113161829..113162386-chr2:97481549..97482238,2	Hela-S3	cervix:
12	chr2:97481562..97482123-chr7:10979299..10980019,2	Hela-S3	cervix:
13	chr2:97481193..97483827-chr2:97615548..97618256,2	MCF-7	breast:
14	chr2:97302401..97304754-chr2:97481583..97484330,2	MCF-7	breast:
15	chr2:97425678..97429518-chr2:97479689..97484495,7	MCF-7	breast:
16	chr2:97481330..97485256-chr2:97521136..97525640,5	K562	blood:
17	chr17:57913918..57915795-chr2:97481404..97483312,2	MCF-7	breast:
18	chr2:97480014..97482644-chr2:97518894..97524629,5	MCF-7	breast:
19	chr2:97481539..97482070-chr4:6695226..6696046,2	Hela-S3	cervix:
20	chr2:97480844..97484629-chr2:97532869..97536982,6	MCF-7	breast:
21	chr2:97481330..97483685-chr2:97521136..97525158,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD23-2	chr2:97480684-97481990	NONHSAT072586

Variant related genes	Relation type
CNNM3	TF binding region
ENSG00000273265	TF binding region
CNNM3	CpG island
ENSG00000273265	CpG island
ENSG00000168754	Chromatin interaction
ENSG00000114331	Chromatin interaction
ENSG00000189043	Chromatin interaction
ENSG00000213337	Chromatin interaction
ENSG00000168758	Chromatin interaction
ENSG00000007341	Chromatin interaction
ENSG00000252845	Chromatin interaction
ENSG00000163993	Chromatin interaction
ENSG00000114982	Chromatin interaction
ENSG00000135976	Chromatin interaction
ENSG00000163126	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000158158	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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	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	nsv874680	chr2:97309574-97678319	Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
8	nsv526313	chr2:97333492-97660619	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
9	nsv874681	chr2:97410949-97577343	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers 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	55 gene(s)	inside rSNPs	diseases
10	nsv874682	chr2:97423626-97567389	Transcr. at gene 5' and 3' Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
11	nsv1009720	chr2:97464803-97522856	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
12	nsv535830	chr2:97464803-97522856	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
13	esv3419974	chr2:97480425-97484723	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	esv3522461	chr2:97480625-97484323	Flanking Active TSS Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	esv3522462	chr2:97481225-97484298	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
16	esv3522464	chr2:97481225-97484298	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 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	chr2:97480800-97482800	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr2:97480800-97483000	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr2:97480800-97483000	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr2:97481000-97482000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:97481000-97482800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:97481000-97482800	Active TSS	Colonic Mucosa	Colon
7	chr2:97481000-97483000	Active TSS	H1 Cell Line	embryonic stem cell
8	chr2:97481000-97483000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:97481000-97483000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:97481000-97483000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:97481000-97483000	Active TSS	Fetal Stomach	stomach
12	chr2:97481000-97483000	Active TSS	Ovary	ovary
13	chr2:97481000-97483000	Active TSS	Psoas Muscle	Psoas
14	chr2:97481000-97483200	Active TSS	H9 Cell Line	embryonic stem cell
15	chr2:97481000-97483400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:97481000-97484000	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr2:97481200-97482800	Active TSS	Right Atrium	heart
18	chr2:97481200-97482800	Active TSS	Right Ventricle	heart
19	chr2:97481200-97483000	Active TSS	iPS-15b Cell Line	embryonic stem cell
20	chr2:97481200-97483000	Active TSS	iPS-18 Cell Line	embryonic stem cell
21	chr2:97481200-97483000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:97481200-97483000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr2:97481200-97483000	Active TSS	Esophagus	oesophagus
24	chr2:97481200-97483000	Active TSS	Gastric	stomach
25	chr2:97481200-97483000	Active TSS	Left Ventricle	heart
26	chr2:97481200-97483000	Active TSS	Lung	lung
27	chr2:97481200-97483000	Active TSS	Sigmoid Colon	Sigmoid Colon
28	chr2:97481200-97483000	Active TSS	Thymus	Thymus
29	chr2:97481200-97483000	Active TSS	NHDF-Ad	bronchial
30	chr2:97481200-97483200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:97481200-97483200	Active TSS	Aorta	Aorta
32	chr2:97481200-97483200	Active TSS	Colon Smooth Muscle	Colon
33	chr2:97481200-97483200	Active TSS	Small Intestine	intestine
34	chr2:97481200-97483200	Active TSS	A549	lung
35	chr2:97481200-97483400	Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr2:97481200-97483400	Active TSS	Hela-S3	cervix
37	chr2:97481200-97483600	Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr2:97481200-97484000	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr2:97481400-97482200	Active TSS	Fetal Kidney	kidney
40	chr2:97481400-97482600	Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr2:97481400-97482800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr2:97481400-97482800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:97481400-97482800	Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr2:97481400-97482800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:97481400-97482800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr2:97481400-97482800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:97481400-97482800	Active TSS	Pancreas	Pancrea
48	chr2:97481400-97482800	Active TSS	Stomach Smooth Muscle	stomach
49	chr2:97481400-97482800	Active TSS	Spleen	Spleen
50	chr2:97481400-97482800	Active TSS	Dnd41	blood

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