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

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EnhancerAtlas ID
HS095-05484 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr11:64333880-64335070 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2078267chr1164334114hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat4MA0518.1chr11:64334872-64334886CCCTTTCCTGGAAG-7.25
ZNF263MA0528.1chr11:64334445-64334466GGAGAAGGGAAGGCAAGGGGA+6.34
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr116433402464334364
chr116433460064335062
Number: 1             
IDChromosomeStartEnd
GH11I064564chr116433218964335552
Enhancer Sequence
TTTAAAAAAC TTCAATTTTT TTCTGATAAA TCAGAAGGAG TGCTCTCACT GCAAACACCC 60
GGGACCAGTT TTTTTTTTTA AAAAAAAAAA AAACCTTCCA GGATTCCTCA GTTCTCCCAG 120
GGGCCGGCTC TGCAACCTTT GTTATTCAAA TCAGAGGCTT TGAAGCTGGT GACCTTGTGG 180
GTTTTCCTGT CTTGTTAACC CAGTTGTTAT CTGTCCAAGG CTCCAGTGTC GGCCGCTTTG 240
AGCACCAGCC CAGTGACTCT CACGTCACTC ACATAAACTT CATGAAACAC CGCGGCTTGT 300
GCGATTTTAC TCTGATGTTG TTGGGCTGGT GTTGTCCGAT GTTTATTGGG TGATGCAATC 360
AGGTGACGCC TAAGGGGAGG GCTGGGAGGA GCATCTGGGT TAAGCAGGGA GAGCACAGAT 420
TTTAAACGTG GCCGAGAAGA ATTTTACCTT GCAGCCAGTT GTGGATCCAA ATCCCATCTC 480
CAAACCATGA GAATTTAAAT ACCGTAAATT CAGCTACTCG TGAGCCAGTG GGGTGGGGGA 540
GTGGGCAGAA AGCAGACCCT GAGATGGAGA AGGGAAGGCA AGGGGAGATG CAGCCACAGC 600
CTGGGCCCAG CCCAGCCCCT GGGAGCGTGG GAGCTGGGGC CTTTCTGGGT GGTCCCTCTG 660
CCCCATGAAC CAGTCACAGG CTGCTCTCCC CAGAGAAGGG GCAGCACTCC CAGGGGCTGG 720
GGGACAGGCT CTCCATCCTG AATGTGGTCT GGGCAATGCA GCCCAGGGTC TCCCGAGAGG 780
CCCTGTCCTG CCATGATTCC CATCTTCCAA GAGAAAGGCA CAGTGTGACT GGTTATCAGA 840
ATCAAAGCCA GAGAGGGCTA GTCCGGAAGT GAGGGGCAGC TCAGAGGCCC CCGAGGGCAG 900
ACTTGGTCCC AGCCAGAGAG GCAACGCCCC AGCGCATCGC TGCCCCTGAC ACAAAGCCTG 960
TGTGTGAAGG GATGGTGGAG CCACCCTGCC TGCCCTTTCC TGGAAGAGCC TGACGCTGGG 1020
GTTGTGTCCT GAGTTTGGCA GGCTTCTGGG ATCGCTGGCC GAGACAAGCC CAGGATTGTC 1080
CTCCGGGGTT GGCCATGTCC TCCCAGGCAG CTCCTGGTGG GAGGTGCTGT TGCTGTTGGG 1140
GTGCCCTCTC CCCGGCAGGG CAGGGACCTG ACTTCCAGCC TTGCCCGCAG 1190