EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS184-14959 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr19:1166690-1168470 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs57813069chr191167157hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr19:1167959-1167980CCCACCCCTCCCACATCCTCC-6.02
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_00709chr19:1164779-1174569Adipose_Nuclei
SE_01009chr19:1164760-1174482Adrenal_Gland
SE_27437chr19:1163884-1174772Esophagus
SE_34735chr19:1165403-1178527HeLa
SE_36707chr19:1167701-1174788HMEC
SE_41641chr19:1166133-1174299LNCaP
SE_44628chr19:1168170-1174545NHDF-Ad
SE_45020chr19:1167784-1170851NHLF
SE_47010chr19:1166731-1170858Ovary
SE_47328chr19:1164729-1173997Panc1
SE_50303chr19:1168244-1174783Sigmoid_Colon
SE_52663chr19:1168249-1170406Small_Intestine
SE_53901chr19:1162363-1175876Spleen
SE_62700chr19:1151017-1215145Tonsil
SE_68758chr19:1166680-1167708H9
SE_68758chr19:1167776-1174885H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1911670511167578
Enhancer Sequence
CTTGAGCCTG TGGTCCCCTC TAACCTACAC GTCTTTTTCT CCTGAGCAGA CGTTAAGCTA 60
AATCCCCACT CACTCCAGAC TTCCGGTCCT TTGAAATGGA GGTGCCCTTG TGTGTCTTCA 120
ATCCATGTGG AGGGTAGTCT GGCCCATCCC ACACCTGCTA CTGTCACTGC CTCACATCAG 180
CGGCCTCAGG CCACAAGGTC TCCCCACCTG GCTCCTTGGG GAGTGCCAAG CGTTGCCAGC 240
AGCCGGGCTA TGCTGATCCC AGACAAGTGG CTCGACCGGT CACCACTGTC CTTGAGCTTA 300
AGTCCAGCCT TGGTGACAAA AATGTCACAA GGACCTGCAT CCGAGCCCTG AGGGCATCAG 360
GTCCTGGAGG AGGAGGAAGA GTCCCTTCTG GCTTCGGGCT GGGCTTGAGG ACGGCAGCTC 420
CAAGACCGCT TAGAGCGAGA CTTCAGCGCT GACTGCTGGA GCTACGCACC CTGTCCTGAC 480
AATGGCCGCA CAGTTAGGCG CTGCTCCACG CCTGGAGGAG GGAACTGAGG GCCCGAAATC 540
ACAGAAGCAG GAACTCCAGG TTCGCCAGTG CGGCCTGATC CACCTTCCCT CAAACGTAGC 600
TGCTGACAAC GACACCCACG CGCCCTCTCT GGGCCCAGCA GGTCAGAGGT CCAGGTGGGC 660
TGGCTGCTCC ACGGCCACGG CTCCAAGGCC AAGGTCAAGG CACTGCTGTC CTGGGCCCTG 720
GTCTGGGTTC TCCGGGAGAG TCCGCGCCTG AGCTCGGCCG GGGGCGGGAT TCTGCTCCCT 780
GTGGCCACTG GGCTGAGGCC CCACTTCCCT GCTTTCGGGG AGCCACGTCC CCCATCACGC 840
CATCCCTCCC TCCTAAAAGC CAGCAGGGCA AGGTCCCTCT TAGGCTTCTG ACCTGACCTC 900
CCCTCCTCCA GCTGGAGAAG GGTCCCACGC ATGAGGACAT TTGTGACGAT GCCGGGACCC 960
GAGGAATCCA GGACGACCCC TCTGCAGAGC CCCTGTGCCC CGGGAGGCAC CACACCCACG 1020
GCTCCAGGGG GTGGGGGGGA CGGTGGCTTC TCTGGGGCTG ACCCAGACCT GCAGTACACA 1080
GCGCCAGGCC ATGAGGTCTC AGCCTGCGGT CAGGCCGCGT GCACGGAAAC CCAGGCTCCT 1140
GAACGGCCAG CCAGGAGCAA AGCCGGCCAC TGAGTACGGG AGCAGGCTCC GGGGACACGC 1200
TCCCACTCCT TTTAGGGGCC CAGAGGCTGT GGATGAGGAG CTCGAGTATC CCCCTCTCAG 1260
TGTAACCTCC CCACCCCTCC CACATCCTCC AAGTGGGGCA GGAGCCGCCT CACCAGAGCT 1320
GGGGGAGGGG GCCACACAGG TGCACCCCTG GGGAGGGGCA GCGGAGACTT GTGGGCAGGA 1380
ATGTGGCCAG GGTTTCTAGA TCATCTGGTT TTTCAAGAGA AGCCACAAGT CTGCGTTTGA 1440
GGGTGGCAGC CCCTGGTGTT CCAAAGTCGG CAAGCAATTC AAGCATCCAC ACCCCCACCC 1500
CGGGGCAGCG TTGGGTGCCC AGACCTCAGG GCCACCCCGA GAGCTCCTGC ATCCACCTGG 1560
GGGCTCGCAG CTCCCCCAAG CTCCTGGCGG GTAGCAGTCA TTCCAGGATC TGATAAAAGC 1620
CCCCGAAAAT GCCCCGGTCA GCCCAGCCAC ACCCGGGCAA CACCGACAGC CATTCTCCAC 1680
CAGGGCCCCA GCGCCCAGCT GAGTGAGACC CACCCGGTAG CTTCCGGGGC TGGGCCCCTG 1740
CCCCACCAGT GAAAACATTC TGGTCACAGT GATGCCGCCC 1780