EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-05845 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr11:68109180-68111780 
TF binding sites/motifs
Number: 6             
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
Number of super-enhancer constituents: 25             
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_24963chr11:68108633-68109647Colon_Crypt_3
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
TTCTTTCCCA GCAAGGCCTG CTCTGTCTCA GGTAGCATGC AGCCCCCCGA CCCACTTCTC 60
ATGTAGCATG CAGCCCCCCG ACCCACTTCA CCCTGCACCA TTTCCCTGAT CTGCAGCGTT 120
TATGATGTAA CATTACTAAG GTGTCCTTAT TGGCTATGTG TATTGCTTGT TTATTACCAC 180
CCACGTGAAT ACGGAGCCAT TCAGGCCGTG TCCTGGGTGT CTGGGTGGGC CAGCTGGTGC 240
TGGGCACTCG CCTGCTGGAG GAGTGAGTGC CCATGGCCAG CCCCTCCTGG TGCCTGGGCT 300
GCGTCTCCTC CTTAGTGTGC TGCCTCTACA GGCTTTTCTC CTGAACTGTC CTCTTTGCTT 360
TTTTTTTTTT TTTTAAGCTT TAAAAGAAGT TTTTGTAGAG ATGCGGTCTT GCTGTGTTGC 420
CCAGGCTGGT CTTGAACTCC TGGCCTGAGA TGATCCTCTC TCCTCGGAAA GTGCTGGGAT 480
TATAGGTGTG AGCTACGGAG CCGGCCCTTC CCTTCTACTC TGCTACTCTG CTGTTCTCTC 540
TCCCTCCCGT CGGGTTCTGC TCCTGCCACG TTCTCCCCTC TCCCCACCAA AGGCTGGGTT 600
TTCTTTGTCA GGGCTCCTTT CCCCTTTGGA GAAGAGGGGG CTGTAGGGCC TTGGTGCGAG 660
GCCCTCCAGT GACAGGATCC CCCATCACCC AGAGTTCCAC AGGCCCTGGT AGGGAGGAGG 720
GGGAGCAGAA GAGGAGGTGC CATCTTTGCC TGCTGGGGAA GGGCAGGGGC CACCCACACA 780
GAGCTCTCCC ATTTGCTGTG GACCCTGGGG CCACTGCCAG TTCCTTCCAA AGGAAAGCCA 840
GCTCCCCAGG TGGTGGGAGA GTGATGTGGC TTCCTCTTAA ACTTAGGAAT TGAGTGTGTG 900
GTTGCTTCTA AGTGCCTTAG AAGCCGGAGC GGCTCCTGGA AAGAGCCTGC CTGCCACAGC 960
GGGCCTTACC CTGGCTGTGC CCACAGATGT CCCTGGGGCC TGCCGCTCCT GCCCGGCTCT 1020
CCTGGCCTCC CCCGGTGTGG GTTGGGAAAA GCACAGCAAA TTAAAAAACA CCTCCATCTC 1080
TGGCCTTTGA AGAATGCATC TGAACAGCCG AGAGTGTAAA CCGTGGTGAA ATGTGGTCTT 1140
TCCAGTTTGG GGAGAAGCAG GGCAGAGCTG GGGCTTTTGT ACCCAGGGTT TCCAAGAGCT 1200
CCTGCCTCCC TCGGCTGGGC TGGCCAGGGC CCCCCGCTGG GACCTCCAGC TGTAATAGGG 1260
AAGGTTTTAC TGGGTTGCTG GCCACTGTGG ACTGCCCCTA AGGGCAGGTA TGCCTGCCTT 1320
TACCCGGGTT CCCCTCCTGC CTGGAAGATA CAGCCCATGG GAGGCCTGTT GTCTGTGGGA 1380
TCCTCCAGCA TCAGAGACAC TGGGGCCAGC GTCTGCCTGG TGAGGTGCAG GCCTGGCAGG 1440
CCCGGTCCCC CACCTGCTTG AGCACCCACG GTGGTGGGGG CTCGCTGCCT CCCGAGACAA 1500
TCTATGTCAT TGTTGTCCAA GGAAGCTAAT TTAGAGTAGA AAGTTCCGTG TCCAGTCCCA 1560
CTCTGTGCGT GTGTTAGCAG GGGACTCTCG GGCCGGAGCT GGGTCCACCC TGGTAGGGGG 1620
ACTTCATGGG GCCTGGGCGA CAGCACTGTG TATTTGTGTG TGTGTGTGTT TGTGTGTGTG 1680
TGTGTCTGAG GAGGTGGACC AGTTTCTCAA AAGGCCTGTG ACCCCAAGAA CCAAGGAATT 1740
TCAGCCTGGG TGGATCACAC CTTCACTGGT GAGTGGGACA AGCTGGGGGC CCTCGCCACA 1800
GGAGCAGCCA GGGCATGGGG CACAGTTGGC CTCATTCACA AAATGGGAGT ATAAGTGATC 1860
CCTGCTCTGG CGGCCAGGAC GATGAGTGGG AACACACCGT GTGGGGGCTG CCTGGCCTGG 1920
GTGTGCCGCG GGTGTCCTTG TTGGTGATGG TTCCACCTGC TTGTGCCACC AGTGCCCTCT 1980
GGGTCTCACA CACAACTCTC TTCCCAGCGA AGGCCCCTCC TGCCCTCAGG CCTCAGTGCT 2040
GCTTCCGTCT CGGAAGGCCC CAGGAGCTCC TGCATCCTGG GCGTGATTCC TGTGTGCCTG 2100
CAGACCCCCT CGCGGCTGCC ATCTCATCCT TTGGTGCACC TGTTGGCCAG ACCTCCTGGT 2160
AGCGGGTGCT GCACTCCCCT GAATGTGCCG GGGCCTGGGG GCAGGGACCT GGGCTCCTCC 2220
CTCACTGAGT GGAGGGAACT CAGTGTCTTG GAGTTGGGGT GCCTGCAGGC TGGGTGGTGC 2280
AGGTGAAATG CAGACCTCTC AGCTGGTGTT CCAGAGCAGC TGCCTTCCCC CGCCCGAGGG 2340
ACTTCACCCG CAGCCCAGTC AGGGGTGGCG CCTGGGTGCA TCGCCCGCAG GCTGGGTAGG 2400
GGTGGAGCCT GGGTGGCCCT GCCTGTGAGC TGCATAGTTG TCGCCTTTGA CCCTGAGTTT 2460
TCTTCGTTAT CTGTTTGGAC CTGTTTGGGG CAGGCAGGGG ATGAGATCTG AAGATAAATG 2520
CCTTAGCTGT GACCATCTCC TTTTGTGAGA GGTCAATGTC CAGTTCCGCT GCAGTTATAA 2580
CATCCCATTT TTTGATTTCT 2600