Variant report

Variant	rs13386878
Chromosome Location	chr2:111435895-111435896
allele	G/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	GTF2F1	chr2:111435640-111436236	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr2:111435197-111436699	ECC-1	luminal epithelium:	n/a	n/a
3	SIN3AK20	chr2:111435090-111436657	HCT-116	colon:	n/a	n/a
4	TAF1	chr2:111435610-111436020	H1-neurons	neurons:	n/a	n/a
5	SP4	chr2:111435532-111435952	H1-hESC	embryonic stem cell:	n/a	chr2:111435770-111435786
6	NRF1	chr2:111435445-111436335	GM12878	blood:	n/a	chr2:111435679-111435690 chr2:111435644-111435655 chr2:111435645-111435659 chr2:111435478-111435487
7	POLR2A	chr2:111435428-111436073	SK-N-MC	brain:	n/a	n/a
8	MXI1	chr2:111434941-111436634	IMR90	lung:	n/a	n/a
9	POLR2A	chr2:111435504-111436082	A549	lung:	n/a	n/a
10	POLR2A	chr2:111435357-111436393	HUVEC	blood vessel:	n/a	n/a
11	REST	chr2:111435703-111435996	A549	lung:	n/a	n/a
12	MAX	chr2:111435626-111435960	K562	blood:	n/a	n/a
13	MXI1	chr2:111435448-111436438	Hela-S3	cervix:	n/a	n/a
14	NFIC	chr2:111435599-111436083	ECC-1	luminal epithelium:	n/a	n/a
15	ZKSCAN1	chr2:111435500-111435941	Hela-S3	cervix:	n/a	n/a
16	ELF1	chr2:111435614-111435945	A549	lung:	n/a	n/a
17	STAT2	chr2:111435588-111436113	K562	blood:	n/a	n/a
18	EP300	chr2:111434930-111437363	K562	blood:	n/a	chr2:111436737-111436746
19	NFATC1	chr2:111435593-111436137	GM12878	blood:	n/a	n/a
20	MAX	chr2:111435352-111436247	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:111435536-111435923	Hela-S3	cervix:	n/a	n/a
22	NRF1	chr2:111435499-111436042	HepG2	liver:	n/a	chr2:111435679-111435690 chr2:111435644-111435655 chr2:111435645-111435659
23	STAT3	chr2:111435635-111435936	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr2:111435199-111436746	U87	brain:	n/a	n/a
25	MBD4	chr2:111435612-111436156	HepG2	liver:	n/a	n/a
26	RCOR1	chr2:111435357-111435963	HepG2	liver:	n/a	n/a
27	SIN3AK20	chr2:111435289-111436063	SK-N-SH	brain:	n/a	n/a
28	MAFK	chr2:111435526-111435976	HepG2	liver:	n/a	n/a
29	NFYA	chr2:111435575-111436086	GM12878	blood:	n/a	chr2:111435710-111435725 chr2:111435710-111435724 chr2:111435709-111435721 chr2:111435712-111435722 chr2:111435680-111435698 chr2:111435710-111435723 chr2:111435684-111435699 chr2:111435710-111435728 chr2:111435710-111435725
30	CHD2	chr2:111435461-111436483	Hela-S3	cervix:	n/a	chr2:111435475-111435485
31	TAF1	chr2:111435249-111436222	K562	blood:	n/a	n/a
32	CHD1	chr2:111434776-111436780	GM12878	blood:	n/a	chr2:111435475-111435485
33	ELK1	chr2:111435807-111436884	K562	blood:	n/a	n/a
34	SP1	chr2:111435281-111436395	HCT-116	colon:	n/a	chr2:111435746-111435760 chr2:111435475-111435484 chr2:111436016-111436025 chr2:111436120-111436133 chr2:111435503-111435517 chr2:111435711-111435732
35	MYC	chr2:111435052-111437318	K562	blood:	n/a	chr2:111435181-111435189
36	TAF1	chr2:111435451-111436020	H1-hESC	embryonic stem cell:	n/a	n/a
37	MAFK	chr2:111435638-111436028	K562	blood:	n/a	n/a
38	TAF1	chr2:111435311-111436008	SK-N-SH	brain:	n/a	n/a
39	MXI1	chr2:111434513-111436697	GM12878	blood:	n/a	n/a
40	MYC	chr2:111435738-111435918	HepG2	liver:	n/a	n/a
41	POLR2A	chr2:111435550-111436115	GM12891	blood:	n/a	n/a
42	POLR2A	chr2:111435469-111436447	GM12892	blood:	n/a	n/a
43	POLR2A	chr2:111435149-111436611	PFSK-1	brain:	n/a	n/a
44	PAX5	chr2:111435509-111435909	GM12878	blood:	n/a	n/a
45	HEY1	chr2:111435386-111436660	K562	blood:	n/a	n/a
46	EP300	chr2:111435620-111436109	GM12878	blood:	n/a	n/a
47	RCOR1	chr2:111435278-111436765	Hela-S3	cervix:	n/a	n/a
48	NFYA	chr2:111435518-111436291	Hela-S3	cervix:	n/a	chr2:111435710-111435725 chr2:111435710-111435724 chr2:111435709-111435721 chr2:111435712-111435722 chr2:111435680-111435698 chr2:111435710-111435723 chr2:111435684-111435699 chr2:111435710-111435728 chr2:111435710-111435725
49	TAL1	chr2:111435429-111437712	K562	blood:	n/a	n/a
50	POLR2A	chr2:111434634-111437160	GM12891	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:111435858-111435908	HEK293	kidney:	embryo
2	chr2:111435850-111435900	NHDF-neo	bronchial:	n/a
3	chr2:111435858-111435908	HRPEpiC	eye:	n/a
4	chr2:111435858-111435908	RPTEC	kidney:	n/a
5	chr2:111435858-111435908	HNPCEpiC	eye:	n/a
6	chr2:111435858-111435908	HCPEpiC	choroid plexus:	n/a
7	chr2:111435858-111435908	HRCEpiC	kidney:	n/a
8	chr2:111435858-111435908	LNCaP	prostate:	n/a
9	chr2:111435858-111435908	AG04449	skin:	fetal
10	chr2:111435858-111435908	GM12878	blood:	n/a
11	chr2:111435858-111435908	HPAEpiC	pulmonary alveolar:	n/a
12	chr2:111435850-111435900	Hepatocyte	liver:	n/a
13	chr2:111435858-111435908	AG09309	skin:	n/a
14	chr2:111435850-111435900	ProgFib	skin:	n/a
15	chr2:111435858-111435908	HEEpiC	esophagus:	n/a
16	chr2:111435858-111435908	Hepatocyte	liver:	n/a
17	chr2:111435850-111435900	LNCaP	prostate:	n/a
18	chr2:111435850-111435900	HCF	heart:	n/a
19	chr2:111435858-111435908	H1-hESC	embryonic stem cell:	embryo
20	chr2:111435850-111435900	BE2_C	brain:	n/a
21	chr2:111435858-111435908	GM06990	blood:	n/a
22	chr2:111435858-111435908	NHBE	bronchial:	n/a
23	chr2:111435850-111435900	HMEC	breast:	n/a
24	chr2:111435850-111435900	ovcar-3	ovarian:	n/a
25	chr2:111435850-111435900	IMR90	lung:	fetal
26	chr2:111435858-111435908	PANC-1	pancreas:	n/a
27	chr2:111435858-111435908	ProgFib	skin:	n/a
28	chr2:111435858-111435908	AG10803	skin:	n/a
29	chr2:111435850-111435900	HEEpiC	esophagus:	n/a
30	chr2:111435858-111435908	MCF-7	breast:	n/a
31	chr2:111435858-111435908	T-47D	breast:	n/a
32	chr2:111435858-111435908	HMEC	breast:	n/a
33	chr2:111435858-111435908	IMR90	lung:	fetal
34	chr2:111435858-111435908	NH-A	brain:	n/a
35	chr2:111435850-111435900	NHBE	bronchial:	n/a
36	chr2:111435850-111435900	ECC-1	luminal epithelium:	n/a
37	chr2:111435850-111435900	H1-hESC	embryonic stem cell:	embryo
38	chr2:111435858-111435908	HAEpiC	amniotic membrane:	n/a
39	chr2:111435850-111435900	AG04450	lung:	fetal
40	chr2:111435850-111435900	SAEC	small airway:	n/a
41	chr2:111435858-111435908	HCT-116	colon:	n/a
42	chr2:111435858-111435908	HIPEpiC	eye:	n/a
43	chr2:111435858-111435908	NB4	blood:	n/a
44	chr2:111435850-111435900	PANC-1	pancreas:	n/a
45	chr2:111435858-111435908	HRE	kidney:	n/a
46	chr2:111435850-111435900	CMK	blood:	n/a
47	chr2:111435858-111435908	AoSMC	blood vessel:	n/a
48	chr2:111435850-111435900	MCF-7	breast:	n/a
49	chr2:111435858-111435908	SK-N-SH_RA	brain:	n/a
50	chr2:111435850-111435900	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:111409847..111412405-chr2:111435701..111437237,2	K562	blood:
2	chr2:111435750..111438683-chr2:111457735..111460578,3	K562	blood:
3	chr2:111434111..111436826-chr2:111878321..111880919,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOXL-3	chr2:111435835-111436174	NONHSAT073228
2	lnc-ACOXL-3	chr2:111435835-111436174	NONHSAT073229

Variant related genes	Relation type
BUB1	TF binding region
BUB1	CpG island
ENSG00000153094	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10175974	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10193862	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10203271	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10204694	1.00[EUR][1000 genomes]
rs11897518	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11900983	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];0.91[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11903773	1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13393728	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13398617	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13410685	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13412647	0.87[AMR][1000 genomes]
rs13415981	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13419537	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13426054	1.00[CEU][hapmap]
rs13430683	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17041553	1.00[TSI][hapmap]
rs17041555	1.00[TSI][hapmap]
rs17041561	1.00[TSI][hapmap]
rs28502311	1.00[EUR][1000 genomes]
rs34026418	1.00[TSI][hapmap]
rs4255970	1.00[CEU][hapmap]
rs58093108	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59372758	1.00[EUR][1000 genomes]
rs66741152	1.00[EUR][1000 genomes]
rs66924117	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6721997	1.00[EUR][1000 genomes]
rs67862961	1.00[EUR][1000 genomes]
rs72828819	1.00[EUR][1000 genomes]
rs72828821	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72828826	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72828829	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72828830	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72942137	0.90[AMR][1000 genomes]
rs7419932	1.00[CEU][hapmap]
rs7581640	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7594746	1.00[EUR][1000 genomes]
rs7609252	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008581	chr2:110826262-111487021	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	esv2751813	chr2:110834561-111447446	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	esv994221	chr2:110847086-111453103	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers 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	47 gene(s)	inside rSNPs	diseases
4	nsv436279	chr2:110850697-111453448	Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv435724	chr2:110851622-111453839	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	esv3502444	chr2:110852415-111453435	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	esv3460817	chr2:110852627-111453192	Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	esv3502445	chr2:110852643-111453216	Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	esv3460819	chr2:110852686-111453177	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	esv3460820	chr2:110852686-111453177	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	esv3502446	chr2:110852704-111453148	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
12	esv3502447	chr2:110852704-111453148	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv874836	chr2:110983050-111463391	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
14	nsv874837	chr2:111367727-111463391	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv582696	chr2:111367727-111469138	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
17	nsv582697	chr2:111386233-111451816	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer 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	3 gene(s)	inside rSNPs	diseases
18	nsv582698	chr2:111387676-111452539	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv874839	chr2:111400934-111868010	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
20	nsv1008758	chr2:111415136-111626467	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
21	nsv535890	chr2:111415136-111626467	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr2:111433000-111436400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:111433000-111436400	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr2:111433400-111436400	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr2:111433800-111436800	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr2:111434000-111436400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:111434200-111436200	Active TSS	iPS-18 Cell Line	embryonic stem cell
7	chr2:111434200-111436200	Active TSS	GM12878-XiMat	blood
8	chr2:111434200-111436400	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr2:111434200-111436400	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr2:111434200-111436400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:111434200-111436400	Active TSS	A549	lung
12	chr2:111434200-111436400	Active TSS	Hela-S3	cervix
13	chr2:111434200-111436600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:111434200-111436600	Active TSS	H9 Cell Line	embryonic stem cell
15	chr2:111434200-111436600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr2:111434200-111436600	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr2:111434200-111436800	Active TSS	H1 Cell Line	embryonic stem cell
18	chr2:111434200-111436800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:111434200-111436800	Active TSS	NHDF-Ad	bronchial
20	chr2:111434200-111437200	Active TSS	K562	blood
21	chr2:111434200-111437200	Active TSS	NHLF	lung
22	chr2:111434400-111436200	Active TSS	HMEC	breast
23	chr2:111434400-111436400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:111434400-111436400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr2:111434400-111436400	Active TSS	Fetal Thymus	thymus
26	chr2:111434400-111436600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
27	chr2:111434400-111436600	Active TSS	Fetal Brain Female	brain
28	chr2:111434600-111436200	Active TSS	Thymus	Thymus
29	chr2:111434600-111436400	Active TSS	Fetal Muscle Leg	muscle
30	chr2:111434600-111436600	Active TSS	Fetal Heart	heart
31	chr2:111434600-111437000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr2:111434600-111437200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr2:111434800-111436200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:111434800-111436400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr2:111434800-111436400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:111434800-111436400	Active TSS	Muscle Satellite Cultured Cells	--
37	chr2:111434800-111436400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:111434800-111436400	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr2:111434800-111436400	Active TSS	Dnd41	blood
40	chr2:111434800-111436600	Bivalent/Poised TSS	HepG2	liver
41	chr2:111434800-111436800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr2:111435000-111436200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:111435000-111436200	Active TSS	NH-A	brain
44	chr2:111435000-111436200	Active TSS	NHEK	skin
45	chr2:111435000-111436400	Active TSS	Placenta Amnion	Placenta Amnion
46	chr2:111435000-111436400	Active TSS	HSMM	muscle
47	chr2:111435000-111436600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr2:111435000-111436600	Active TSS	Fetal Brain Male	brain
49	chr2:111435000-111436600	Active TSS	Fetal Kidney	kidney
50	chr2:111435000-111436800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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