EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS110-00688 
Organism
Homo sapiens 
Tissue/cell
KATO3 
Coordinate
chr11:68109570-68112180 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Hnf4aMA0114.3chr11:68111728-68111744GAGGTCAATGTCCAGT+6.03
SNAI2MA0745.2chr11:68111314-68111324TGCACCTGTT-6.02
ZIC1MA0696.1chr11:68110407-68110421GGCCCCCCGCTGGG+6.57
ZIC3MA0697.1chr11:68110407-68110422GGCCCCCCGCTGGGA+6.45
ZIC4MA0751.1chr11:68110407-68110422GGCCCCCCGCTGGGA+7
ZNF263MA0528.1chr11:68109892-68109913GGAGGAGGGGGAGCAGAAGAG+7.94
ZfxMA0146.2chr11:68112031-68112045CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_01084chr11:68109649-68111647Adrenal_Gland
SE_01626chr11:68108163-68111814Aorta
SE_23171chr11:68109562-68110811Colon_Crypt_1
SE_23171chr11:68110947-68111547Colon_Crypt_1
SE_23847chr11:68109972-68110288Colon_Crypt_2
SE_23847chr11:68110289-68110654Colon_Crypt_2
SE_23847chr11:68110829-68111470Colon_Crypt_2
SE_24963chr11:68109707-68111781Colon_Crypt_3
SE_26848chr11:68108540-68111692Esophagus
SE_28000chr11:68109037-68111683Fetal_Intestine
SE_28937chr11:68108999-68111817Fetal_Intestine_Large
SE_30440chr11:68109627-68110542Fetal_Muscle
SE_31879chr11:68108601-68111508Gastric
SE_41339chr11:68109304-68111760Left_Ventricle
SE_41686chr11:68108545-68111755LNCaP
SE_42205chr11:68108279-68111936Lung
SE_47270chr11:68107065-68111537Panc1
SE_47593chr11:68109331-68111557Pancreas
SE_48658chr11:68108510-68111875Right_Atrium
SE_52526chr11:68109557-68111667Small_Intestine
SE_54745chr11:68108562-68111696Stomach_Smooth_Muscle
SE_56733chr11:68108677-68111762VACO_400
SE_65630chr11:68108334-68111699Pancreatic_islets
SE_68821chr11:68108478-68111751H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr116811160268111710
chr116810960368110809
chr116811118168111448
Number: 1             
IDChromosomeStartEnd
GH11I068340chr116810769168112525
Enhancer Sequence
TTTTGTAGAG ATGCGGTCTT GCTGTGTTGC CCAGGCTGGT CTTGAACTCC TGGCCTGAGA 60
TGATCCTCTC TCCTCGGAAA GTGCTGGGAT TATAGGTGTG AGCTACGGAG CCGGCCCTTC 120
CCTTCTACTC TGCTACTCTG CTGTTCTCTC TCCCTCCCGT CGGGTTCTGC TCCTGCCACG 180
TTCTCCCCTC TCCCCACCAA AGGCTGGGTT TTCTTTGTCA GGGCTCCTTT CCCCTTTGGA 240
GAAGAGGGGG CTGTAGGGCC TTGGTGCGAG GCCCTCCAGT GACAGGATCC CCCATCACCC 300
AGAGTTCCAC AGGCCCTGGT AGGGAGGAGG GGGAGCAGAA GAGGAGGTGC CATCTTTGCC 360
TGCTGGGGAA GGGCAGGGGC CACCCACACA GAGCTCTCCC ATTTGCTGTG GACCCTGGGG 420
CCACTGCCAG TTCCTTCCAA AGGAAAGCCA GCTCCCCAGG TGGTGGGAGA GTGATGTGGC 480
TTCCTCTTAA ACTTAGGAAT TGAGTGTGTG GTTGCTTCTA AGTGCCTTAG AAGCCGGAGC 540
GGCTCCTGGA AAGAGCCTGC CTGCCACAGC GGGCCTTACC CTGGCTGTGC CCACAGATGT 600
CCCTGGGGCC TGCCGCTCCT GCCCGGCTCT CCTGGCCTCC CCCGGTGTGG GTTGGGAAAA 660
GCACAGCAAA TTAAAAAACA CCTCCATCTC TGGCCTTTGA AGAATGCATC TGAACAGCCG 720
AGAGTGTAAA CCGTGGTGAA ATGTGGTCTT TCCAGTTTGG GGAGAAGCAG GGCAGAGCTG 780
GGGCTTTTGT ACCCAGGGTT TCCAAGAGCT CCTGCCTCCC TCGGCTGGGC TGGCCAGGGC 840
CCCCCGCTGG GACCTCCAGC TGTAATAGGG AAGGTTTTAC TGGGTTGCTG GCCACTGTGG 900
ACTGCCCCTA AGGGCAGGTA TGCCTGCCTT TACCCGGGTT CCCCTCCTGC CTGGAAGATA 960
CAGCCCATGG GAGGCCTGTT GTCTGTGGGA TCCTCCAGCA TCAGAGACAC TGGGGCCAGC 1020
GTCTGCCTGG TGAGGTGCAG GCCTGGCAGG CCCGGTCCCC CACCTGCTTG AGCACCCACG 1080
GTGGTGGGGG CTCGCTGCCT CCCGAGACAA TCTATGTCAT TGTTGTCCAA GGAAGCTAAT 1140
TTAGAGTAGA AAGTTCCGTG TCCAGTCCCA CTCTGTGCGT GTGTTAGCAG GGGACTCTCG 1200
GGCCGGAGCT GGGTCCACCC TGGTAGGGGG ACTTCATGGG GCCTGGGCGA CAGCACTGTG 1260
TATTTGTGTG TGTGTGTGTT TGTGTGTGTG TGTGTCTGAG GAGGTGGACC AGTTTCTCAA 1320
AAGGCCTGTG ACCCCAAGAA CCAAGGAATT TCAGCCTGGG TGGATCACAC CTTCACTGGT 1380
GAGTGGGACA AGCTGGGGGC CCTCGCCACA GGAGCAGCCA GGGCATGGGG CACAGTTGGC 1440
CTCATTCACA AAATGGGAGT ATAAGTGATC CCTGCTCTGG CGGCCAGGAC GATGAGTGGG 1500
AACACACCGT GTGGGGGCTG CCTGGCCTGG GTGTGCCGCG GGTGTCCTTG TTGGTGATGG 1560
TTCCACCTGC TTGTGCCACC AGTGCCCTCT GGGTCTCACA CACAACTCTC TTCCCAGCGA 1620
AGGCCCCTCC TGCCCTCAGG CCTCAGTGCT GCTTCCGTCT CGGAAGGCCC CAGGAGCTCC 1680
TGCATCCTGG GCGTGATTCC TGTGTGCCTG CAGACCCCCT CGCGGCTGCC ATCTCATCCT 1740
TTGGTGCACC TGTTGGCCAG ACCTCCTGGT AGCGGGTGCT GCACTCCCCT GAATGTGCCG 1800
GGGCCTGGGG GCAGGGACCT GGGCTCCTCC CTCACTGAGT GGAGGGAACT CAGTGTCTTG 1860
GAGTTGGGGT GCCTGCAGGC TGGGTGGTGC AGGTGAAATG CAGACCTCTC AGCTGGTGTT 1920
CCAGAGCAGC TGCCTTCCCC CGCCCGAGGG ACTTCACCCG CAGCCCAGTC AGGGGTGGCG 1980
CCTGGGTGCA TCGCCCGCAG GCTGGGTAGG GGTGGAGCCT GGGTGGCCCT GCCTGTGAGC 2040
TGCATAGTTG TCGCCTTTGA CCCTGAGTTT TCTTCGTTAT CTGTTTGGAC CTGTTTGGGG 2100
CAGGCAGGGG ATGAGATCTG AAGATAAATG CCTTAGCTGT GACCATCTCC TTTTGTGAGA 2160
GGTCAATGTC CAGTTCCGCT GCAGTTATAA CATCCCATTT TTTGATTTCT TTTTATTTTT 2220
TCCTTTTTCT TTTTGAGATG GAGTCTCGCT CTGTCACCCA GGCTGGAGTG CAATGGGGTG 2280
ACCTCAGCTC ACTGCAACCT CCACTTCTCG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC 2340
TGACTAGCAG GGGTTACAGG CGTGAGCCAC CACGCCCCAG CTAATTTTTG TATTTTTAGT 2400
AGAGGCAAGG TTTCGTCATG TTGGCCAGGC TGGTCTCAAA CTCCTGGCCT TAAGTGATCT 2460
GCCCGCCTCG GCCTCCCAAA GTGCTGAGAT GACAGGTGTG AGCCACCGTG CCCGGCCCAG 2520
AACTCTTTAA TTCCCACCTG AAACTTGCCG CCTTAAGCAG GTCCCCAGTC TCCCTCCCCT 2580
AGTCCCTGGT CCCACCATTC TGCTTTCTGT 2610