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

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EnhancerAtlas ID
HS148-03978 
Organism
Homo sapiens 
Tissue/cell
NHLF 
Coordinate
chr12:25767510-25768650 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUNMA0488.1chr12:25768142-25768155AAGATGAGGTCAT+6.54
JUNMA0488.1chr12:25767921-25767934ATGACATCATTTT-7.22
JUND(var.2)MA0492.1chr12:25768141-25768156GAAGATGAGGTCATT+6.32
JUND(var.2)MA0492.1chr12:25767920-25767935AATGACATCATTTTT-7.2
MEF2CMA0497.1chr12:25768564-25768579TTCTATTTTTGGTAG-6.43
Nfe2l2MA0150.2chr12:25768170-25768185GACCATGAGTCAGCA+6.58
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr122576774625768642
Number: 1             
IDChromosomeStartEnd
GH12I025614chr122576746825768770
Enhancer Sequence
AGTTTTCAGA AACCCAAAAG AGAACAGTAT TTCTCTTCTG TTAACAGAGG TTAACTGCGG 60
TAGAACAGAC TTGGCAGATT GCAGAGTCTA GCACCTTGGG AGACAGAATC AGACTTGAAA 120
GTGTGCTTGG CAAATAGGGA AAGTGGCTAT ATTAGTTTGC TAAGGCTGCC ACAACAAAGT 180
ATCACAGACT GGGTGACCTA AACAACAGAA ATTTATTTTC TCATACTTCT GGAAACTGGA 240
AGTCCAAGAC CAAGGTATTG TTAGGTTTGG TTTGTTTCTT CTGAGGCTCT TCTTGGCTTA 300
AAGATGGCCA TCTTCTCCCT GTTTTCACAC TGTCTTCCCT CTGTTGATGT CTGGGTTCTA 360
ATCGCCTCTT CTTATAAGGT CATTAGTCAT ATTGGATTAA GGCCCAATCT AATGACATCA 420
TTTTTAATTA ATTACCTTTG TTGAGACCCT ATCTGCATCA CCGTCACAAT CTGAGGTACT 480
GGGGGAAAGG ACGTCAACCG ATAAATACAG GGGGGCACAA TCCAGCCTGT AATAGTGGCC 540
AAACAAAATG AGGCTCAGCT AAAAGGGAGA AATTTAGGTA GCAGAACAAG CTTCTTGCTC 600
ACGAGATGAG AGATGGGGAT GGGTGAATGC AGAAGATGAG GTCATTGTGG GTCACATGCT 660
GACCATGAGT CAGCAACATG GTGCAGTAAA ACACATGAGC ACAATTCCTG GATATAGAAA 720
TAGGAGAAGC AGAGTAGAGT GTGTGAGGTA ATTCAGTTCC CTTTGCAGTA ATTGGAAGCA 780
CCTTTCCAAT TCTGAACTCC AAGCCAGAGA AGGTTGTGAA GATTCTGGAC AACGTTCAGA 840
AGAGAGCCAT ATAGCAGAAC CATATCCTTT TTTTAATTTT TTAATTTTTT TTTTTGAGAC 900
ATGGTCTCAC TCTTTACTCT TGTCGCCCAG GTTGCAGTAG AGTGGCATGA TCTGGGCTCA 960
CTGCAACCTT TGCCTTCCAG ACTGAAGCGA TCCTCCTGCC TCAGCTTCCT CAGTAGCTGA 1020
GATTCAGGTG TGTGCCACCA CACCCAGCTA ATTTTTCTAT TTTTGGTAGA GACAGGGTTT 1080
CAACATGTTG CCCAGGCTGG TCTCAAACTT CTGAGTTCAA GCGATCTGCC TGCCTTGGCC 1140