Variant report

Variant	rs28384426
Chromosome Location	chr13:111267758-111267759
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBL1XR1	chr13:111267415-111268116	GM12878	blood:	n/a	n/a
2	POLR2A	chr13:111267491-111268257	GM12878	blood:	n/a	n/a
3	STAT1	chr13:111267753-111268001	GM12878	blood:	n/a	n/a
4	YY1	chr13:111267628-111268367	ECC-1	luminal epithelium:	n/a	n/a
5	POLR2A	chr13:111267529-111268686	H1-neurons	neurons:	n/a	n/a
6	POLR2A	chr13:111267582-111268198	U87	brain:	n/a	n/a
7	POLR2A	chr13:111267393-111268915	GM12878	blood:	n/a	n/a
8	RCOR1	chr13:111267667-111268257	GM12878	blood:	n/a	n/a
9	POLR2A	chr13:111267393-111268307	U87	brain:	n/a	n/a
10	CBX3	chr13:111267552-111268003	K562	blood:	n/a	n/a
11	TCF12	chr13:111267711-111268080	GM12878	blood:	n/a	n/a
12	STAT3	chr13:111267758-111267958	MCF10A-Er-Src	breast:	n/a	n/a
13	CHD1	chr13:111267549-111268261	GM12878	blood:	n/a	n/a
14	TEAD4	chr13:111267731-111268204	ECC-1	luminal epithelium:	n/a	n/a
15	BRCA1	chr13:111267579-111268094	Hela-S3	cervix:	n/a	n/a
16	ZNF143	chr13:111267591-111268141	H1-hESC	embryonic stem cell:	n/a	n/a
17	GABPA	chr13:111267408-111268682	K562	blood:	n/a	n/a
18	REST	chr13:111267272-111268911	H1-neurons	neurons:	n/a	chr13:111268313-111268326
19	ZNF143	chr13:111267572-111268197	K562	blood:	n/a	n/a
20	GABPA	chr13:111267424-111268243	A549	lung:	n/a	n/a
21	POLR2A	chr13:111267608-111268774	GM10847	blood:	n/a	n/a
22	E2F6	chr13:111267109-111268247	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr13:111267603-111268245	A549	lung:	n/a	n/a
24	SP1	chr13:111267486-111268134	A549	lung:	n/a	n/a
25	RUNX3	chr13:111267543-111268276	GM12878	blood:	n/a	chr13:111268127-111268142
26	EP300	chr13:111267524-111268006	GM12878	blood:	n/a	n/a
27	MAX	chr13:111267553-111268215	MCF-7	breast:	n/a	n/a
28	POLR2A	chr13:111267634-111268284	A549	lung:	n/a	n/a
29	YY1	chr13:111267612-111268097	SK-N-SH_RA	brain:	n/a	n/a
30	CHD2	chr13:111267696-111268037	HepG2	liver:	n/a	n/a
31	POLR2A	chr13:111267192-111268599	SK-N-MC	brain:	n/a	n/a
32	TBL1XR1	chr13:111267535-111267958	K562	blood:	n/a	n/a
33	TAF1	chr13:111267590-111268298	Hela-S3	cervix:	n/a	n/a
34	CCNT2	chr13:111267717-111268787	K562	blood:	n/a	n/a
35	TAF1	chr13:111267709-111268177	H1-neurons	neurons:	n/a	n/a
36	CREB1	chr13:111267713-111268123	A549	lung:	n/a	n/a
37	YY1	chr13:111267711-111268083	GM12891	blood:	n/a	n/a
38	EGR1	chr13:111267707-111268073	K562	blood:	n/a	chr13:111267857-111267871
39	USF2	chr13:111267623-111267996	Hela-S3	cervix:	n/a	n/a
40	MYBL2	chr13:111267519-111268109	HepG2	liver:	n/a	n/a
41	RCOR1	chr13:111267744-111268082	K562	blood:	n/a	n/a
42	MAX	chr13:111267466-111268193	A549	lung:	n/a	n/a
43	PBX3	chr13:111267369-111268151	SK-N-SH	brain:	n/a	chr13:111267785-111267805
44	POLR2A	chr13:111267571-111268221	Raji	blood:	n/a	n/a
45	POLR2A	chr13:111267442-111268122	SK-N-SH	brain:	n/a	n/a
46	ELF1	chr13:111267576-111268133	HepG2	liver:	n/a	chr13:111267858-111267867 chr13:111267872-111267885
47	BHLHE40	chr13:111267534-111268165	HepG2	liver:	n/a	n/a
48	EBF1	chr13:111267725-111267889	GM12878	blood:	n/a	n/a
49	POLR2A	chr13:111267582-111268252	K562	blood:	n/a	n/a
50	POLR2A	chr13:111267617-111268926	GM12878	blood:	n/a	n/a

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:111266678..111269187-chr13:111295319..111298212,3	MCF-7	breast:
2	chr13:111266655..111268705-chr13:111294879..111298471,3	K562	blood:
3	chr13:111266587..111269692-chr13:111357018..111359356,4	K562	blood:
4	chr13:111265515..111270086-chr13:111364987..111368051,5	MCF-7	breast:
5	chr13:111267350..111267981-chr17:56756502..56757440,2	NB4	blood:
6	chr13:111267620..111268282-chr20:46130126..46130887,2	Hela-S3	cervix:
7	chr13:111266965..111271727-chr13:111364973..111369025,9	MCF-7	breast:
8	chr13:111266746..111269387-chr13:111357064..111359748,3	MCF-7	breast:
9	chr13:111267596..111269197-chr13:111364131..111366094,2	K562	blood:
10	chr13:111267467..111269967-chr13:111564590..111568374,3	MCF-7	breast:
11	chr13:111267252..111268156-chr8:144635373..144636016,2	HCT-116	colon:
12	chr13:111267645..111268224-chr17:7747085..7747789,2	Hela-S3	cervix:
13	chr13:111266944..111268705-chr13:111296076..111298471,2	K562	blood:
14	chr12:50677315..50677913-chr13:111267621..111268237,2	Hela-S3	cervix:
15	chr13:111267631..111268254-chr5:108083564..108084113,2	Hela-S3	cervix:
16	chr13:111265756..111270693-chr13:111363417..111370660,10	K562	blood:
17	chr13:111266737..111268751-chr13:111366724..111368921,2	K562	blood:

No data

Variant related genes	Relation type
CARKD	TF binding region
ENSG00000134905	Chromatin interaction
ENSG00000088448	Chromatin interaction
ENSG00000132510	Chromatin interaction
ENSG00000151422	Chromatin interaction
ENSG00000153487	Chromatin interaction
ENSG00000124151	Chromatin interaction
ENSG00000200997	Chromatin interaction
ENSG00000104518	Chromatin interaction
ENSG00000050405	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1041143	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1041173	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11069855	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11069856	0.82[JPT][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11620520	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12428965	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12429905	1.00[CEU][hapmap];0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12430333	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12583083	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1853861	0.80[JPT][hapmap]
rs2011692	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2148081	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2274411	0.91[AFR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3742193	1.00[CEU][hapmap];0.86[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[TSI][hapmap];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3742194	1.00[CEU][hapmap];0.86[CHB][hapmap];0.87[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.92[TSI][hapmap];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3742196	1.00[CEU][hapmap];0.86[CHB][hapmap];0.90[JPT][hapmap];0.91[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3783097	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3825465	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3825466	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3825467	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4771700	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4771701	0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4771702	0.80[JPT][hapmap]
rs4771703	0.80[JPT][hapmap];1.00[MKK][hapmap]
rs4771704	0.80[JPT][hapmap]
rs4773230	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4773232	0.80[JPT][hapmap]
rs61103246	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72661645	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72661647	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72661650	0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72661656	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72661657	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7322067	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7323602	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7981194	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7981780	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7991671	0.82[ASN][1000 genomes]
rs7995119	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9583513	0.80[ASN][1000 genomes]
rs9583514	0.80[ASN][1000 genomes]
rs9583518	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9583520	0.80[JPT][hapmap]
rs9588207	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9588209	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9588214	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[CHD][hapmap];0.92[GIH][hapmap];0.90[JPT][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046423	chr13:110936104-111286607	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv832720	chr13:111100235-111295993	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv1044234	chr13:111143053-111370580	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	216 gene(s)	inside rSNPs	diseases
4	nsv949634	chr13:111151460-111582996	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
5	nsv901010	chr13:111165390-111286592	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Strong 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	23 gene(s)	inside rSNPs	diseases
6	nsv1053922	chr13:111167764-111330876	Flanking Active TSS Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
7	nsv1043849	chr13:111167764-111340418	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription 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 target site	25 gene(s)	inside rSNPs	diseases
8	nsv541924	chr13:111167764-111340418	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1036160	chr13:111167764-111347308	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv541925	chr13:111167764-111347308	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv901011	chr13:111168951-111280002	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases
12	nsv901012	chr13:111220842-111340342	Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
13	nsv1038089	chr13:111229517-111274823	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
14	nsv1044340	chr13:111234073-111692994	Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	240 gene(s)	inside rSNPs	diseases
15	nsv563123	chr13:111237260-111292044	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
16	nsv525124	chr13:111261267-111280002	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
17	nsv563124	chr13:111261267-111300943	Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS 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 target site	17 gene(s)	inside rSNPs	diseases
18	nsv1048700	chr13:111265350-111658617	Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	240 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs28384426	GRTP1	cis	cerebellum	SCAN
rs28384426	AL139385.1	cis	Muscle Skeletal	GTEx
rs28384426	PCID2	cis	cerebellum	SCAN
rs28384426	CARKD	cis	Muscle Skeletal	GTEx
rs28384426	CARKD	cis	parietal	SCAN
rs28384426	CARKD	cis	cerebellum	SCAN
rs28384426	TUBGCP3	cis	parietal	SCAN
rs28384426	TNFSF13B	cis	cerebellum	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111265200-111267800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr13:111267000-111267800	ZNF genes & repeats	Fetal Intestine Small	intestine
3	chr13:111267000-111267800	Flanking Active TSS	Dnd41	blood
4	chr13:111267000-111269000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:111267200-111267800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr13:111267200-111267800	Flanking Active TSS	Brain Hippocampus Middle	brain
7	chr13:111267200-111267800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
8	chr13:111267200-111267800	Enhancers	Fetal Heart	heart
9	chr13:111267200-111267800	Flanking Active TSS	Stomach Smooth Muscle	stomach
10	chr13:111267200-111267800	Enhancers	Spleen	Spleen
11	chr13:111267200-111267800	Flanking Active TSS	GM12878-XiMat	blood
12	chr13:111267200-111267800	Flanking Active TSS	HepG2	liver
13	chr13:111267200-111268000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr13:111267200-111268000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr13:111267200-111268600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr13:111267200-111268800	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr13:111267200-111268800	Active TSS	Brain Anterior Caudate	brain
18	chr13:111267200-111268800	Active TSS	HSMMtube	muscle
19	chr13:111267200-111268800	Active TSS	NHLF	lung
20	chr13:111267200-111269000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr13:111267200-111269000	Active TSS	Rectal Smooth Muscle	rectum
22	chr13:111267200-111269400	Active TSS	A549	lung
23	chr13:111267200-111270000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:111267400-111267800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr13:111267400-111267800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:111267400-111267800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:111267400-111267800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr13:111267400-111267800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr13:111267400-111267800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr13:111267400-111267800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr13:111267400-111267800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr13:111267400-111267800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr13:111267400-111267800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
34	chr13:111267400-111267800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr13:111267400-111267800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr13:111267400-111267800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr13:111267400-111267800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr13:111267400-111267800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr13:111267400-111267800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
40	chr13:111267400-111267800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr13:111267400-111267800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr13:111267400-111267800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr13:111267400-111267800	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr13:111267400-111267800	Flanking Active TSS	Brain Cingulate Gyrus	brain
45	chr13:111267400-111267800	Flanking Active TSS	Brain Substantia Nigra	brain
46	chr13:111267400-111267800	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr13:111267400-111267800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
48	chr13:111267400-111267800	Flanking Active TSS	Fetal Kidney	kidney
49	chr13:111267400-111267800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
50	chr13:111267400-111267800	Flanking Active TSS	Fetal Muscle Leg	muscle

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