Variant report

Variant	rs201280849
Chromosome Location	chr6:26199963-26199964
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:319)
CpG islands
(count:0)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TAF1	chr6:26198960-26199993	PFSK-1	brain:	n/a	n/a
2	POLR2A	chr6:26198429-26200562	Raji	blood:	n/a	n/a
3	POLR2A	chr6:26198413-26200653	H1-neurons	neurons:	n/a	n/a
4	SIN3A	chr6:26198741-26200085	GM12878	blood:	n/a	n/a
5	POLR2A	chr6:26198093-26200571	SK-N-SH	brain:	n/a	n/a
6	POLR2A	chr6:26193825-26201103	K562	blood:	n/a	n/a
7	CEBPD	chr6:26197958-26200955	K562	blood:	n/a	chr6:26199490-26199501
8	CREB1	chr6:26198433-26200072	HepG2	liver:	n/a	n/a
9	POLR2A	chr6:26199281-26200008	HepG2	liver:	n/a	n/a
10	TAF1	chr6:26199044-26200181	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr6:26187684-26208312	K562	blood:	n/a	n/a
12	POLR2A	chr6:26195351-26200889	H1-hESC	embryonic stem cell:	n/a	n/a
13	UBTF	chr6:26198050-26200726	K562	blood:	n/a	n/a
14	TAF1	chr6:26199019-26200419	K562	blood:	n/a	n/a
15	POLR2A	chr6:26198447-26200465	HEK293	kidney:	n/a	n/a
16	ATF2	chr6:26194955-26200949	H1-hESC	embryonic stem cell:	n/a	n/a
17	TBL1XR1	chr6:26199036-26200818	K562	blood:	n/a	n/a
18	BCLAF1	chr6:26198316-26200518	GM12878	blood:	n/a	n/a
19	MAX	chr6:26199553-26200374	K562	blood:	n/a	n/a
20	SIN3AK20	chr6:26198407-26200001	HCT-116	colon:	n/a	n/a
21	TAF7	chr6:26198846-26200685	K562	blood:	n/a	n/a
22	BCLAF1	chr6:26192611-26200894	K562	blood:	n/a	n/a
23	CEBPD	chr6:26199616-26200219	HepG2	liver:	n/a	n/a
24	SIN3AK20	chr6:26199619-26200190	HepG2	liver:	n/a	n/a
25	NFATC1	chr6:26198406-26200626	GM12878	blood:	n/a	n/a
26	MAZ	chr6:26199305-26200523	GM12878	blood:	n/a	n/a
27	POLR2A	chr6:26198228-26200565	GM18951	blood:	n/a	n/a
28	TCF7L2	chr6:26199206-26199984	HCT-116	colon:	n/a	n/a
29	POLR2A	chr6:26196587-26200011	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr6:26198003-26200608	GM12891	blood:	n/a	n/a
31	POLR2A	chr6:26198308-26200543	HCT-116	colon:	n/a	n/a
32	FOSL2	chr6:26199261-26200205	HepG2	liver:	n/a	chr6:26199581-26199590
33	POLR2A	chr6:26198134-26200533	IMR90	lung:	n/a	n/a
34	RCOR1	chr6:26198104-26200756	Hela-S3	cervix:	n/a	n/a
35	TCF12	chr6:26199053-26200103	SK-N-SH	brain:	n/a	n/a
36	BHLHE40	chr6:26199319-26200552	K562	blood:	n/a	n/a
37	FOXA1	chr6:26199158-26200035	HepG2	liver:	n/a	n/a
38	POLR2A	chr6:26198489-26200462	GM12878	blood:	n/a	n/a
39	GTF2B	chr6:26199255-26200053	K562	blood:	n/a	n/a
40	MYC	chr6:26199881-26200100	MCF-7	breast:	n/a	n/a
41	TBP	chr6:26199166-26199993	K562	blood:	n/a	n/a
42	ZBTB33	chr6:26198941-26200295	HepG2	liver:	n/a	n/a
43	POLR2A	chr6:26195548-26200603	U87	brain:	n/a	n/a
44	RUNX3	chr6:26198418-26200539	GM12878	blood:	n/a	n/a
45	ELK1	chr6:26199162-26200050	K562	blood:	n/a	n/a
46	POLR2A	chr6:26197958-26200590	PFSK-1	brain:	n/a	n/a
47	PML	chr6:26193184-26200952	K562	blood:	n/a	n/a
48	MXI1	chr6:26199063-26200338	HepG2	liver:	n/a	n/a
49	POLR2A	chr6:26197989-26200787	Hela-S3	cervix:	n/a	n/a
50	MTA3	chr6:26198166-26200713	GM12878	blood:	n/a	n/a

No data

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:169073988..169075864-chr6:26199270..26200811,2	MCF-7	breast:
2	chr6:26199071..26200007-chr6:26216694..26217540,4	Hela-S3	cervix:
3	chr19:19773987..19774730-chr6:26199521..26200292,2	Hela-S3	cervix:
4	chr6:26197296..26200583-chr6:27100054..27103203,5	MCF-7	breast:
5	chr6:26198554..26200175-chr6:26536662..26538943,2	K562	blood:
6	chr11:67055725..67056438-chr6:26199156..26199993,2	NB4	blood:
7	chr11:62554047..62556731-chr6:26198828..26201701,2	K562	blood:
8	chr6:26044090..26046416-chr6:26198004..26201095,3	MCF-7	breast:
9	chr6:26198756..26200403-chr6:27791864..27793365,2	K562	blood:
10	chr6:26198322..26200388-chr6:26537916..26540393,2	K562	blood:
11	chr1:109234344..109235208-chr6:26199482..26200409,2	Hela-S3	cervix:
12	chr6:26158344..26159047-chr6:26199394..26200119,2	NB4	blood:
13	chr6:26124286..26124791-chr6:26199350..26200021,2	Hela-S3	cervix:
14	chr6:26196435..26200575-chr6:27099094..27104350,6	MCF-7	breast:
15	chr6:26030021..26034897-chr6:26196138..26201230,10	MCF-7	breast:
16	chr6:26196890..26209578-chr6:27096615..27108451,46	K562	blood:
17	chr17:60966442..60968338-chr6:26199786..26201613,2	MCF-7	breast:
18	chr6:26198124..26199998-chr6:26520705..26522799,2	K562	blood:
19	chr6:26196862..26203126-chr6:27774221..27779033,8	MCF-7	breast:
20	chr17:36412759..36413334-chr6:26199517..26200071,2	Hela-S3	cervix:
21	chr6:26198976..26200690-chr8:144396916..144399356,2	MCF-7	breast:
22	chr6:26193858..26202011-chr6:27112529..27117825,14	K562	blood:
23	chr6:26195075..26199998-chr6:26518402..26523264,7	K562	blood:
24	chr6:3157349..3159256-chr6:26198220..26201219,2	K562	blood:
25	chr6:26199734..26202965-chr6:27114829..27116362,3	MCF-7	breast:
26	chr6:17582130..17584573-chr6:26197697..26200325,2	MCF-7	breast:
27	chr5:79950077..79950796-chr6:26199069..26200065,2	NB4	blood:
28	chr6:26195729..26208268-chr6:27092660..27105612,50	K562	blood:
29	chr1:45185248..45187840-chr6:26198016..26200996,2	K562	blood:
30	chr6:26199481..26200204-chr6:27114324..27114900,2	NB4	blood:
31	chr6:26199305..26201035-chr6:27856541..27859187,2	K562	blood:
32	chr6:26199788..26200550-chr7:5565555..5566318,2	Hela-S3	cervix:
33	chr20:43976860..43977457-chr6:26199521..26200409,2	Hela-S3	cervix:
34	chr6:26197661..26200522-chr9:91932409..91933987,2	MCF-7	breast:
35	chr6:26199067..26201068-chr7:44834709..44838117,3	K562	blood:
36	chr6:26199830..26202146-chr6:26537922..26540846,2	MCF-7	breast:
37	chr6:26195849..26201222-chr6:27858647..27864324,7	K562	blood:
38	chr17:39845714..39848067-chr6:26197980..26200504,2	MCF-7	breast:
39	chr6:26198554..26201743-chr6:27781165..27784293,4	MCF-7	breast:
40	chr6:26198826..26200652-chr6:27777401..27778996,2	K562	blood:
41	chr6:26198160..26200179-chr6:33280182..33281976,2	MCF-7	breast:
42	chr6:26054507..26059193-chr6:26196981..26201593,9	MCF-7	breast:
43	chr6:26197637..26200453-chr6:27859195..27862304,3	MCF-7	breast:
44	chr2:10952393..10953142-chr6:26199873..26200745,2	Hela-S3	cervix:
45	chr17:59477149..59479351-chr6:26199135..26202043,2	MCF-7	breast:
46	chr6:26016695..26019436-chr6:26198057..26199976,2	MCF-7	breast:
47	chr18:61636924..61637774-chr6:26199598..26200501,2	Hela-S3	cervix:
48	chr19:13261047..13261585-chr6:26199496..26200267,2	Hela-S3	cervix:
49	chr1:149859325..149861103-chr6:26197923..26200886,2	MCF-7	breast:
50	chr6:26197916..26207803-chr6:27772547..27779655,13	K562	blood:

No data

Variant related genes	Relation type
HIST1H4E	TF binding region
HIST1H2AD	TF binding region
ENSG00000217275	TF binding region
HIST1H3D	TF binding region
ENSG00000203813	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000263660	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000199377	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000269176	Chromatin interaction
ENSG00000124610	Chromatin interaction
ENSG00000184428	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000218359	Chromatin interaction
ENSG00000198339	Chromatin interaction
ENSG00000217862	Chromatin interaction
ENSG00000134186	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000124145	Chromatin interaction
ENSG00000187742	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000231925	Chromatin interaction
ENSG00000174093	Chromatin interaction
ENSG00000166401	Chromatin interaction
ENSG00000199289	Chromatin interaction
ENSG00000234816	Chromatin interaction
ENSG00000160888	Chromatin interaction
ENSG00000238279	Chromatin interaction
ENSG00000267131	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000104915	Chromatin interaction
ENSG00000143870	Chromatin interaction
ENSG00000197238	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000137267	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000143153	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000196787	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000105726	Chromatin interaction
ENSG00000133316	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000113318	Chromatin interaction
ENSG00000196532	Chromatin interaction
ENSG00000173812	Chromatin interaction
ENSG00000196262	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000228716	Chromatin interaction
ENSG00000185475	Chromatin interaction
ENSG00000121068	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000180573	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26194200-26200600	Active TSS	GM12878-XiMat	blood
2	chr6:26194800-26201000	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr6:26195000-26200400	Active TSS	Aorta	Aorta
4	chr6:26195000-26200400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr6:26195000-26200600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:26195000-26200800	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr6:26195000-26200800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:26195000-26200800	Active TSS	NHDF-Ad	bronchial
9	chr6:26195200-26200000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr6:26195200-26200000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
11	chr6:26195200-26200000	Active TSS	NHLF	lung
12	chr6:26195200-26200600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:26195200-26200600	Active TSS	Brain Angular Gyrus	brain
14	chr6:26195200-26200800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr6:26195200-26201000	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr6:26195200-26201400	Active TSS	H1 Cell Line	embryonic stem cell
17	chr6:26195400-26200000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr6:26195400-26200600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:26195400-26200800	Active TSS	H9 Cell Line	embryonic stem cell
20	chr6:26195400-26200800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:26195400-26200800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:26195400-26200800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:26195400-26200800	Active TSS	Hela-S3	cervix
24	chr6:26195600-26200600	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr6:26195600-26200800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr6:26195600-26201000	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr6:26195600-26201600	Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:26195800-26200600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:26196000-26201400	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr6:26196200-26200400	Active TSS	HSMMtube	muscle
31	chr6:26196800-26200000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr6:26196800-26200000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr6:26196800-26200200	Active TSS	Fetal Intestine Large	intestine
34	chr6:26196800-26200800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:26197000-26200000	Active TSS	Brain Hippocampus Middle	brain
36	chr6:26197000-26200200	Active TSS	Primary T killer memory cells from peripheral blood	blood
37	chr6:26197000-26200200	Active TSS	Brain Germinal Matrix	brain
38	chr6:26197000-26200200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr6:26197000-26200400	Active TSS	Colon Smooth Muscle	Colon
40	chr6:26197200-26200200	Active TSS	Fetal Intestine Small	intestine
41	chr6:26197200-26200200	Active TSS	Right Ventricle	heart
42	chr6:26197200-26200600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:26197200-26200600	Active TSS	Fetal Stomach	stomach
44	chr6:26197200-26200800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:26197200-26200800	Active TSS	Brain Cingulate Gyrus	brain
46	chr6:26197200-26200800	Active TSS	Fetal Brain Male	brain
47	chr6:26197200-26201000	Active TSS	Fetal Thymus	thymus
48	chr6:26197400-26200000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:26197400-26200000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:26197400-26200200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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