Variant report

Variant	rs73736559
Chromosome Location	chr6:26200630-26200631
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:0)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26198413-26200653	H1-neurons	neurons:	n/a	n/a
2	POLR2A	chr6:26193825-26201103	K562	blood:	n/a	n/a
3	CEBPD	chr6:26197958-26200955	K562	blood:	n/a	chr6:26199490-26199501
4	POLR2A	chr6:26187684-26208312	K562	blood:	n/a	n/a
5	POLR2A	chr6:26195351-26200889	H1-hESC	embryonic stem cell:	n/a	n/a
6	UBTF	chr6:26198050-26200726	K562	blood:	n/a	n/a
7	ATF2	chr6:26194955-26200949	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr6:26200601-26200744	SK-N-SH	brain:	n/a	n/a
9	TBL1XR1	chr6:26199036-26200818	K562	blood:	n/a	n/a
10	FOS	chr6:26200410-26200683	MCF10A-Er-Src	breast:	n/a	n/a
11	TAF7	chr6:26198846-26200685	K562	blood:	n/a	n/a
12	BCLAF1	chr6:26192611-26200894	K562	blood:	n/a	n/a
13	FOS	chr6:26200423-26200689	MCF10A-Er-Src	breast:	n/a	n/a
14	RCOR1	chr6:26198104-26200756	Hela-S3	cervix:	n/a	n/a
15	SPI1	chr6:26200582-26200885	HL-60	blood:	n/a	n/a
16	PML	chr6:26193184-26200952	K562	blood:	n/a	n/a
17	POLR2A	chr6:26197989-26200787	Hela-S3	cervix:	n/a	n/a
18	MTA3	chr6:26198166-26200713	GM12878	blood:	n/a	n/a
19	SIN3A	chr6:26200598-26200641	GM12878	blood:	n/a	n/a
20	PML	chr6:26197818-26200639	K562	blood:	n/a	n/a
21	RELA	chr6:26198903-26200747	GM12878	blood:	n/a	n/a
22	TAF7	chr6:26194455-26200989	H1-hESC	embryonic stem cell:	n/a	n/a
23	TEAD4	chr6:26193268-26200973	K562	blood:	n/a	n/a
24	POLR2A	chr6:26198077-26200936	K562	blood:	n/a	n/a
25	NFIC	chr6:26195431-26200718	GM12878	blood:	n/a	chr6:26195653-26195669
26	POLR2A	chr6:26198195-26200807	GM19099	blood:	n/a	n/a
27	POLR2A	chr6:26195341-26200934	HL-60	blood:	n/a	n/a
28	TRIM28	chr6:26198908-26200652	K562	blood:	n/a	n/a
29	POLR2A	chr6:26195326-26200683	GM12878	blood:	n/a	n/a
30	POLR2A	chr6:26197995-26200880	GM12878	blood:	n/a	n/a
31	CCNT2	chr6:26200441-26200764	K562	blood:	n/a	n/a
32	POLR2A	chr6:26192524-26200729	K562	blood:	n/a	n/a
33	CHD1	chr6:26194887-26201053	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr6:26200605-26200771	H1-hESC	embryonic stem cell:	n/a	n/a
35	TEAD4	chr6:26198105-26200670	HepG2	liver:	n/a	n/a
36	ATF2	chr6:26199254-26200630	GM12878	blood:	n/a	n/a
37	MYBL2	chr6:26195379-26200666	HepG2	liver:	n/a	n/a
38	POLR2A	chr6:26198205-26200730	GM12892	blood:	n/a	n/a
39	MXI1	chr6:26200274-26200849	K562	blood:	n/a	n/a
40	HEY1	chr6:26195348-26200765	HepG2	liver:	n/a	n/a
41	HEY1	chr6:26198076-26200718	HepG2	liver:	n/a	n/a
42	BCLAF1	chr6:26198223-26200649	GM12878	blood:	n/a	n/a
43	IRF1	chr6:26200282-26200702	K562	blood:	n/a	n/a
44	POU2F2	chr6:26198325-26200659	GM12878	blood:	n/a	chr6:26199633-26199640 chr6:26199630-26199642 chr6:26198534-26198556 chr6:26199631-26199641 chr6:26198407-26198425 chr6:26199632-26199642 chr6:26198862-26198875 chr6:26198411-26198421 chr6:26199630-26199644 chr6:26199632-26199643 chr6:26199629-26199642 chr6:26199628-26199646 chr6:26198410-26198421 chr6:26198539-26198554 chr6:26199632-26199641 chr6:26198409-26198424 chr6:26199630-26199643 chr6:26199631-26199641 chr6:26199629-26199644 chr6:26198405-26198427 chr6:26198862-26198875 chr6:26199633-26199641 chr6:26199632-26199643
45	SIN3AK20	chr6:26195230-26200729	MCF-7	breast:	n/a	n/a
46	POLR2A	chr6:26197985-26200818	SK-N-MC	brain:	n/a	n/a
47	ZKSCAN1	chr6:26198380-26200678	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr6:26194980-26200859	SK-N-MC	brain:	n/a	n/a
49	MTA3	chr6:26195090-26200828	GM12878	blood:	n/a	n/a
50	FOS	chr6:26200354-26200891	MCF10A-Er-Src	breast:	n/a	n/a

No data

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169073988..169075864-chr6:26199270..26200811,2	MCF-7	breast:
2	chr11:62554047..62556731-chr6:26198828..26201701,2	K562	blood:
3	chr6:26044090..26046416-chr6:26198004..26201095,3	MCF-7	breast:
4	chr6:26030021..26034897-chr6:26196138..26201230,10	MCF-7	breast:
5	chr6:26196890..26209578-chr6:27096615..27108451,46	K562	blood:
6	chr17:60966442..60968338-chr6:26199786..26201613,2	MCF-7	breast:
7	chr6:26196862..26203126-chr6:27774221..27779033,8	MCF-7	breast:
8	chr6:26200533..26202173-chr6:36952474..36954550,2	K562	blood:
9	chr6:26198976..26200690-chr8:144396916..144399356,2	MCF-7	breast:
10	chr6:26193858..26202011-chr6:27112529..27117825,14	K562	blood:
11	chr6:3157349..3159256-chr6:26198220..26201219,2	K562	blood:
12	chr6:26199734..26202965-chr6:27114829..27116362,3	MCF-7	breast:
13	chr6:26195729..26208268-chr6:27092660..27105612,50	K562	blood:
14	chr1:45185248..45187840-chr6:26198016..26200996,2	K562	blood:
15	chr6:26199305..26201035-chr6:27856541..27859187,2	K562	blood:
16	chr4:41217852..41218468-chr6:26200103..26200767,2	Hela-S3	cervix:
17	chr6:26200001..26200839-chr7:35076809..35077567,2	Hela-S3	cervix:
18	chr6:26199067..26201068-chr7:44834709..44838117,3	K562	blood:
19	chr6:26199830..26202146-chr6:26537922..26540846,2	MCF-7	breast:
20	chr6:26195849..26201222-chr6:27858647..27864324,7	K562	blood:
21	chr12:54674206..54674730-chr6:26200514..26201138,2	Hela-S3	cervix:
22	chr6:26198554..26201743-chr6:27781165..27784293,4	MCF-7	breast:
23	chr6:26198826..26200652-chr6:27777401..27778996,2	K562	blood:
24	chr6:26054507..26059193-chr6:26196981..26201593,9	MCF-7	breast:
25	chr2:10952393..10953142-chr6:26199873..26200745,2	Hela-S3	cervix:
26	chr17:59477149..59479351-chr6:26199135..26202043,2	MCF-7	breast:
27	chr1:149859325..149861103-chr6:26197923..26200886,2	MCF-7	breast:
28	chr6:26197916..26207803-chr6:27772547..27779655,13	K562	blood:
29	chr6:26196234..26202173-chr6:27109710..27116918,20	K562	blood:
30	chr6:26200530..26203137-chr6:27861093..27863102,2	MCF-7	breast:
31	chr6:26197700..26201009-chr6:27106361..27108760,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000217275	TF binding region
HIST1H4E	TF binding region
HIST1H3D	TF binding region
HIST1H2AD	TF binding region
ENSG00000137409	Chromatin interaction
ENSG00000198339	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000217862	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000184428	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000135486	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000234816	Chromatin interaction
ENSG00000203813	Chromatin interaction
ENSG00000143153	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000196262	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000137267	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000143870	Chromatin interaction
ENSG00000263660	Chromatin interaction
ENSG00000196532	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs41266825	1.00[EUR][1000 genomes]
rs55674533	1.00[EUR][1000 genomes]
rs56049309	1.00[EUR][1000 genomes]
rs59620817	1.00[EUR][1000 genomes]
rs73397366	1.00[EUR][1000 genomes]
rs73736553	1.00[EUR][1000 genomes]
rs73736555	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73736560	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73736561	1.00[EUR][1000 genomes]
rs73736562	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73736566	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73736574	1.00[EUR][1000 genomes]
rs73736577	1.00[EUR][1000 genomes]
rs73736578	1.00[EUR][1000 genomes]
rs73736580	1.00[EUR][1000 genomes]
rs73736581	1.00[EUR][1000 genomes]
rs73736582	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	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers 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	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised 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	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
13	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
14	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
15	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
16	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
17	nsv518431	chr6:26148311-26211368	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
18	nsv526456	chr6:26148311-26211368	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	521 gene(s)	inside rSNPs	diseases
19	nsv883490	chr6:26172219-26231608	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	316 gene(s)	inside rSNPs	diseases
20	nsv1021294	chr6:26190316-26246784	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	309 gene(s)	inside rSNPs	diseases
21	nsv969356	chr6:26199899-26204393	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	85 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26194800-26201000	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr6:26195000-26200800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr6:26195000-26200800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:26195000-26200800	Active TSS	NHDF-Ad	bronchial
5	chr6:26195200-26200800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr6:26195200-26201000	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr6:26195200-26201400	Active TSS	H1 Cell Line	embryonic stem cell
8	chr6:26195400-26200800	Active TSS	H9 Cell Line	embryonic stem cell
9	chr6:26195400-26200800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr6:26195400-26200800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:26195400-26200800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr6:26195400-26200800	Active TSS	Hela-S3	cervix
13	chr6:26195600-26200800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:26195600-26201000	Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr6:26195600-26201600	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr6:26196000-26201400	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr6:26196800-26200800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:26197200-26200800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:26197200-26200800	Active TSS	Brain Cingulate Gyrus	brain
20	chr6:26197200-26200800	Active TSS	Fetal Brain Male	brain
21	chr6:26197200-26201000	Active TSS	Fetal Thymus	thymus
22	chr6:26197600-26200800	Active TSS	Brain Anterior Caudate	brain
23	chr6:26197600-26201200	Active TSS	Thymus	Thymus
24	chr6:26197800-26200800	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr6:26198400-26200800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
26	chr6:26198400-26201600	Active TSS	K562	blood
27	chr6:26199400-26200800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr6:26199600-26200800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:26199800-26200800	Flanking Active TSS	Primary B cells from peripheral blood	blood
30	chr6:26199800-26200800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
31	chr6:26199800-26200800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr6:26199800-26200800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:26199800-26200800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
34	chr6:26199800-26200800	Flanking Active TSS	HUVEC	blood vessel
35	chr6:26199800-26200800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr6:26199800-26200800	Flanking Active TSS	NHEK	skin
37	chr6:26199800-26201000	Flanking Active TSS	Primary hematopoietic stem cells	blood
38	chr6:26200000-26200800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:26200000-26200800	Flanking Active TSS	NHLF	lung
40	chr6:26200200-26200800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:26200200-26200800	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr6:26200200-26200800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr6:26200200-26200800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
44	chr6:26200200-26200800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:26200200-26200800	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr6:26200200-26200800	Flanking Active TSS	Duodenum Mucosa	Duodenum
47	chr6:26200200-26200800	Flanking Active TSS	Fetal Brain Female	brain
48	chr6:26200200-26200800	Flanking Active TSS	Fetal Intestine Large	intestine
49	chr6:26200200-26200800	Flanking Active TSS	Fetal Intestine Small	intestine
50	chr6:26200200-26200800	Flanking Active TSS	Fetal Kidney	kidney

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