Variant report

Variant	rs674400
Chromosome Location	chr11:65188327-65188328
allele	A/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	TCF12	chr11:65188309-65198397	SK-N-SH	brain:	n/a	chr11:65189820-65189828
2	POLR2A	chr11:65187337-65188452	HCT-116	colon:	n/a	n/a
3	CHD1	chr11:65183014-65218224	IMR90	lung:	n/a	chr11:65189696-65189706 chr11:65213009-65213016
4	POLR2A	chr11:65182982-65199920	Hela-S3	cervix:	n/a	n/a
5	GATA1	chr11:65188173-65198061	PBDE	blood:	n/a	chr11:65194820-65194837 chr11:65194824-65194845 chr11:65194831-65194838 chr11:65194829-65194839 chr11:65194829-65194838
6	POLR2A	chr11:65185765-65189757	GM12892	blood:	n/a	n/a
7	POLR2A	chr11:65184755-65189855	GM12892	blood:	n/a	n/a
8	POLR2A	chr11:65188228-65189951	GM12891	blood:	n/a	n/a
9	MYC	chr11:65188156-65188360	MCF10A-Er-Src	breast:	n/a	n/a
10	POLR2A	chr11:65184966-65198365	GM12892	blood:	n/a	n/a
11	NFIC	chr11:65188293-65196290	GM12878	blood:	n/a	chr11:65192369-65192385 chr11:65192369-65192386
12	GATA3	chr11:65188253-65189047	T-47D	breast:	n/a	n/a
13	JUND	chr11:65188204-65198793	SK-N-SH	brain:	n/a	chr11:65188449-65188458 chr11:65197695-65197704 chr11:65189724-65189733 chr11:65189926-65189935 chr11:65195841-65195853 chr11:65189694-65189703
14	POLR2A	chr11:65185731-65204623	U87	brain:	n/a	n/a
15	POLR2A	chr11:65188290-65199915	PANC-1	pancreas:	n/a	n/a
16	POLR2A	chr11:65188321-65189320	GM12891	blood:	n/a	n/a
17	NR2F2	chr11:65188265-65196287	K562	blood:	n/a	n/a
18	POLR2A	chr11:65184867-65198324	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:65182298-65198746	GM12878	blood:	n/a	n/a
20	SP1	chr11:65188267-65196387	HCT-116	colon:	n/a	chr11:65189697-65189707 chr11:65188670-65188680 chr11:65189697-65189711 chr11:65189923-65189935 chr11:65189311-65189325 chr11:65189697-65189706 chr11:65189933-65189943 chr11:65192397-65192411 chr11:65189312-65189321 chr11:65189932-65189944 chr11:65189696-65189708 chr11:65189697-65189706 chr11:65189933-65189943 chr11:65190900-65190913 chr11:65189696-65189708 chr11:65189697-65189707 chr11:65194254-65194275 chr11:65189698-65189707
21	CHD1	chr11:65188301-65198346	GM12878	blood:	n/a	chr11:65189696-65189706
22	POLR2A	chr11:65184718-65196445	HL-60	blood:	n/a	n/a
23	POLR2A	chr11:65185731-65204601	U87	brain:	n/a	n/a
24	SIN3AK20	chr11:65188149-65196500	MCF-7	breast:	n/a	n/a
25	MXI1	chr11:65188160-65198411	SK-N-SH	brain:	n/a	chr11:65194580-65194589 chr11:65188957-65188972
26	POLR2A	chr11:65185871-65189886	U87	brain:	n/a	n/a
27	POLR2A	chr11:65185928-65189829	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:65178313-65199265	PANC-1	pancreas:	n/a	n/a
29	STAT5A	chr11:65188200-65199389	GM12878	blood:	n/a	chr11:65192349-65192361 chr11:65189313-65189325 chr11:65190205-65190213 chr11:65190157-65190169 chr11:65195738-65195749
30	SIN3AK20	chr11:65188273-65196484	HCT-116	colon:	n/a	n/a
31	POLR2A	chr11:65184926-65198709	GM12878	blood:	n/a	n/a
32	POLR2A	chr11:65188327-65199948	PBDE	blood:	n/a	n/a
33	SP1	chr11:65188278-65196386	A549	lung:	n/a	chr11:65189697-65189707 chr11:65188670-65188680 chr11:65189697-65189711 chr11:65189923-65189935 chr11:65189311-65189325 chr11:65189697-65189706 chr11:65189933-65189943 chr11:65192397-65192411 chr11:65189312-65189321 chr11:65189932-65189944 chr11:65189696-65189708 chr11:65189697-65189706 chr11:65189933-65189943 chr11:65190900-65190913 chr11:65189696-65189708 chr11:65189697-65189707 chr11:65194254-65194275 chr11:65189698-65189707
34	POLR2A	chr11:65188054-65198362	GM12892	blood:	n/a	n/a
35	GATA3	chr11:65188300-65188604	SH-SY5Y	brain:	n/a	n/a
36	PML	chr11:65188157-65198451	GM12878	blood:	n/a	chr11:65189628-65189636 chr11:65195222-65195230
37	POLR2A	chr11:65188303-65204577	SK-N-SH	brain:	n/a	n/a
38	NFATC1	chr11:65188283-65189356	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:65185809-65189887	HepG2	liver:	n/a	n/a
40	MTA3	chr11:65182457-65199360	GM12878	blood:	n/a	n/a
41	POLR2A	chr11:65185408-65199253	GM12878	blood:	n/a	n/a
42	POLR2A	chr11:65184993-65198340	K562	blood:	n/a	n/a
43	POLR2A	chr11:65185330-65196319	GM12878	blood:	n/a	n/a
44	POLR2A	chr11:65185430-65207951	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr11:65188307-65189858	GM12891	blood:	n/a	n/a
46	SP1	chr11:65188263-65196287	A549	lung:	n/a	chr11:65189697-65189707 chr11:65188670-65188680 chr11:65189697-65189711 chr11:65189923-65189935 chr11:65189311-65189325 chr11:65189697-65189706 chr11:65189933-65189943 chr11:65192397-65192411 chr11:65189312-65189321 chr11:65189932-65189944 chr11:65189696-65189708 chr11:65189697-65189706 chr11:65189933-65189943 chr11:65190900-65190913 chr11:65189696-65189708 chr11:65189697-65189707 chr11:65194254-65194275 chr11:65189698-65189707
47	WRNIP1	chr11:65187605-65189717	GM12878	blood:	n/a	n/a
48	HEY1	chr11:65187207-65189845	HepG2	liver:	n/a	chr11:65189543-65189558 chr11:65189725-65189734 chr11:65189809-65189824 chr11:65189723-65189732
49	GATA3	chr11:65188169-65189274	MCF-7	breast:	n/a	n/a
50	GATA2	chr11:65188240-65189045	HUVEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:65188099..65190744-chr14:77494274..77497074,3	MCF-7	breast:
2	chr11:64545114..64546892-chr11:65188018..65190269,2	K562	blood:
3	chr1:23885328..23885985-chr11:65188284..65188988,2	Hela-S3	cervix:
4	chr11:65187744..65191441-chr11:65307194..65309813,3	MCF-7	breast:
5	chr11:65186803..65188372-chr7:80548581..80551559,2	MCF-7	breast:
6	chr11:65188258..65192947-chr11:65311570..65315780,5	MCF-7	breast:
7	chr11:65188146..65188840-chr19:13950653..13951548,2	Hela-S3	cervix:
8	chr11:65188178..65189840-chr11:65370838..65373215,2	MCF-7	breast:
9	chr11:65186463..65188700-chr11:65666574..65669229,2	K562	blood:
10	chr11:65186095..65189808-chr11:65319853..65322686,3	MCF-7	breast:
11	chr11:65027099..65029284-chr11:65187685..65190495,2	MCF-7	breast:
12	chr11:65186294..65191468-chr11:65379126..65384544,8	MCF-7	breast:
13	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:
14	chr11:65183635..65190622-chr11:65305653..65310980,8	MCF-7	breast:
15	chr11:65184392..65191686-chr11:65339528..65345365,10	K562	blood:
16	chr11:64544570..64546892-chr11:65186918..65189518,2	K562	blood:
17	chr11:65188021..65191759-chr11:65338955..65343877,5	MCF-7	breast:
18	chr11:65186040..65189423-chr11:65316425..65320462,4	MCF-7	breast:
19	chr11:65187654..65189531-chr5:172755721..172758429,2	MCF-7	breast:
20	chr11:65187484..65190433-chr7:75931597..75933590,2	MCF-7	breast:
21	chr11:65184371..65196984-chr11:65316952..65328208,29	K562	blood:
22	chr11:65182317..65198249-chr11:65333937..65346467,45	MCF-7	breast:
23	chr11:65107573..65110262-chr11:65186195..65188738,2	MCF-7	breast:
24	chr11:65186090..65188584-chr5:68640496..68642731,2	MCF-7	breast:
25	chr11:65098368..65100448-chr11:65187507..65189022,2	K562	blood:
26	chr11:65187686..65190825-chr11:65382299..65384886,3	K562	blood:
27	chr11:65186378..65188992-chr11:65308325..65312434,3	K562	blood:
28	chr11:64644555..64646404-chr11:65186434..65188538,2	MCF-7	breast:
29	chr11:65185186..65203592-chr11:65286522..65299399,55	K562	blood:
30	chr11:65187359..65190548-chr17:56735338..56738257,3	MCF-7	breast:
31	chr11:65187299..65189043-chr6:26156025..26158848,2	K562	blood:
32	chr11:65185945..65193560-chr11:65336627..65344485,19	K562	blood:
33	chr11:64007618..64009808-chr11:65187530..65189288,2	MCF-7	breast:
34	chr11:65187907..65189514-chr11:65336699..65338237,2	K562	blood:
35	chr11:65187300..65188965-chr11:65420277..65421827,2	MCF-7	breast:
36	chr11:65188010..65190276-chr2:43452851..43454855,2	MCF-7	breast:

Variant related genes	Relation type
NEAT1	TF binding region
ENSG00000133884	Chromatin interaction
ENSG00000173327	Chromatin interaction
ENSG00000014138	Chromatin interaction
ENSG00000117318	Chromatin interaction
ENSG00000260233	Chromatin interaction
ENSG00000119669	Chromatin interaction
ENSG00000173465	Chromatin interaction
ENSG00000152518	Chromatin interaction
ENSG00000197136	Chromatin interaction
ENSG00000175592	Chromatin interaction
ENSG00000168066	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000173442	Chromatin interaction
ENSG00000158373	Chromatin interaction
ENSG00000270526	Chromatin interaction
ENSG00000110047	Chromatin interaction
ENSG00000269038	Chromatin interaction
ENSG00000113739	Chromatin interaction
ENSG00000173486	Chromatin interaction
ENSG00000270117	Chromatin interaction
ENSG00000168298	Chromatin interaction
ENSG00000251562	Chromatin interaction
ENSG00000142186	Chromatin interaction
ENSG00000106211	Chromatin interaction
ENSG00000168056	Chromatin interaction
ENSG00000173727	Chromatin interaction
ENSG00000075223	Chromatin interaction
ENSG00000176973	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2957266	0.90[AFR][1000 genomes]
rs3015963	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs472852	0.97[AFR][1000 genomes]
rs635411	1.00[AMR][1000 genomes]
rs643997	0.83[AMR][1000 genomes]
rs7111083	0.97[AFR][1000 genomes];0.83[AMR][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	nsv526181	chr11:64638041-65257329	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1539 gene(s)	inside rSNPs	diseases
2	esv2422285	chr11:65013294-65254540	Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	474 gene(s)	inside rSNPs	diseases
3	nsv897715	chr11:65083491-65427346	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
4	nsv897716	chr11:65083491-65481166	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	999 gene(s)	inside rSNPs	diseases
5	nsv541065	chr11:65117387-65271894	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	835 gene(s)	inside rSNPs	diseases
6	esv1829999	chr11:65136686-65343124	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	963 gene(s)	inside rSNPs	diseases
7	nsv897717	chr11:65140209-65278461	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	942 gene(s)	inside rSNPs	diseases
8	nsv897718	chr11:65140209-65577516	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer 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	1003 gene(s)	inside rSNPs	diseases
9	nsv541066	chr11:65142779-65271894	Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers 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	833 gene(s)	inside rSNPs	diseases
10	nsv541067	chr11:65142779-65313799	Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	950 gene(s)	inside rSNPs	diseases
11	nsv541068	chr11:65142779-65331136	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	953 gene(s)	inside rSNPs	diseases
12	nsv541069	chr11:65142779-65368787	Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	965 gene(s)	inside rSNPs	diseases
13	nsv541070	chr11:65142779-65397058	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	972 gene(s)	inside rSNPs	diseases
14	nsv541071	chr11:65142779-65429352	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	984 gene(s)	inside rSNPs	diseases
15	nsv897719	chr11:65157094-65335705	Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
16	nsv541072	chr11:65171202-65313799	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	946 gene(s)	inside rSNPs	diseases
17	nsv541073	chr11:65171202-65331136	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	949 gene(s)	inside rSNPs	diseases
18	nsv541074	chr11:65171202-65368787	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	961 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	chr11:65181400-65189400	Weak transcription	Ovary	ovary
2	chr11:65182200-65189600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
3	chr11:65182400-65188600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr11:65183000-65189200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:65183000-65189400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:65183400-65188600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr11:65183400-65188600	Flanking Active TSS	Hela-S3	cervix
8	chr11:65183400-65189200	Flanking Active TSS	Brain Anterior Caudate	brain
9	chr11:65183400-65189200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
10	chr11:65183400-65189400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
11	chr11:65183400-65189400	Flanking Active TSS	Stomach Smooth Muscle	stomach
12	chr11:65183400-65189600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr11:65183400-65189600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:65183400-65190200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:65183600-65188600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
16	chr11:65183600-65188600	Flanking Active TSS	Adipose Nuclei	Adipose
17	chr11:65183600-65188600	Flanking Active TSS	Colonic Mucosa	Colon
18	chr11:65183600-65188600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr11:65183600-65189000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:65183600-65189200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:65183600-65189400	Flanking Active TSS	GM12878-XiMat	blood
22	chr11:65183600-65189600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr11:65183600-65189600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr11:65183600-65189600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
25	chr11:65183600-65189600	Flanking Active TSS	Dnd41	blood
26	chr11:65183600-65189800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr11:65183600-65194200	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr11:65183800-65188600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
29	chr11:65183800-65188800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:65183800-65189600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
31	chr11:65183800-65189600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr11:65184000-65189200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr11:65184200-65188800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr11:65185200-65189200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr11:65185200-65189200	Flanking Active TSS	Primary T cells from cord blood	blood
36	chr11:65185200-65189200	Flanking Active TSS	K562	blood
37	chr11:65185800-65189400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:65186000-65188600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr11:65186000-65188600	Flanking Active TSS	NHLF	lung
40	chr11:65186000-65189600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:65186000-65189600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr11:65186000-65193800	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr11:65186000-65195000	Transcr. at gene 5' and 3'	Duodenum Smooth Muscle	Duodenum
44	chr11:65186200-65189400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:65186200-65189400	Weak transcription	Gastric	stomach
46	chr11:65186200-65192400	Active TSS	Right Ventricle	heart
47	chr11:65186200-65197400	Active TSS	Psoas Muscle	Psoas
48	chr11:65186600-65188600	Flanking Active TSS	A549	lung
49	chr11:65186600-65188800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr11:65186600-65189000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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