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

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EnhancerAtlas ID
HS133-26216 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr6:7057990-7059030 
Target genes
Number: 3             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs525678chr67058857hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAFFMA0495.3chr6:7057993-7058008ACGCTGACTCAGCAC+7.23
MAFFMA0495.3chr6:7057993-7058008ACGCTGACTCAGCAC-7.37
MAFGMA0659.1chr6:7057990-7058011GATACGCTGACTCAGCACTGT+7.16
MAFGMA0659.1chr6:7057990-7058011GATACGCTGACTCAGCACTGT-7.46
MAFKMA0496.2chr6:7057991-7058010ATACGCTGACTCAGCACTG+6.3
MAFKMA0496.2chr6:7057991-7058010ATACGCTGACTCAGCACTG-6.7
NFE2L1MA0089.2chr6:7057994-7058009CGCTGACTCAGCACT+6.04
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_24394chr6:7058333-7058889Colon_Crypt_2
SE_25100chr6:7058304-7059442Colon_Crypt_3
SE_27407chr6:7056440-7060972Esophagus
SE_32364chr6:7058086-7059572Gastric
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr670587647058925
Number: 1             
IDChromosomeStartEnd
GH06I007056chr670571147062089
Enhancer Sequence
GATACGCTGA CTCAGCACTG TTCCAACCAA GTGCTTTAAC CCAGCGGCTC CCTAACCTGC 60
CTCATCAGAT TAAGAGGCCG CACCACATAG TTGTTGCACC AGAATCTCCT GGGCCAGCAG 120
TCCATTTTTT TTTTTTTTTT TTTTTTGAGA CAGAGTCTCG CTCTATCACC AGACTGGAGT 180
GCAGTGGCGC GATCTCGGCT CACTGCAACC TCCACCTCCT GGGTTCAAGT GATTCTCCTG 240
CCTCAGCCTC CCGAGTAGCT GGGACTACAG GCGCGTGCCA CCATGCCCAG CTAAGTTTTG 300
TATATTTAGT AGAGACAAGG TTTCGCCACG TTGGCCAGGC TGGTCTCCGT CTCTTGACCT 360
CAAGTGATCC ACCCGCCTGG GCCTCCCAAA GTGCCAGGAT TATGGGCATG AGCCACCGTG 420
CCCAGCCAGT CTGTATTTTT AATAAGCTTT ACAGGTCACT CCGGTATGGA TCATTTTGGG 480
GAACCAGTTT CTTAGCTAGT TTGTTGTAGA GCCTGAGACC TTCCCGTGAG ACCTCCTATG 540
TCTCTCCCAG GGAGAGAAAG AGCTCAAACT TTTTATGAGT TCGTTTCAAC CTGTCCTTTT 600
GCTTTTGTAT ATGATGGACG GTCATTGATA GTGGTGCTCA AAGTTGTTTT TATCCAGATG 660
ACCTGCTGCT TTCCAAATTT AGCACTGGTC TGAAAGAGTG GAGGGATGTG TCAGAAGTCC 720
TCTGCCCTGC TGCTAGGCTG GAAGGAGATT TGGGTTGAAG AGCTATGTGG AGAGTGGAGA 780
GTGACTCAAA CTTTGTACAT TGAAGCTTGT TGGAATGATG CAATCACCCA GGCATTGGAC 840
AGACCACTTC CTGTACCTTT GGATACACAG ACCCAGGGTG TGGTATTTGG CAGTACTCTC 900
AGGAGTAGGC TGGCTGATCC TCTTCAAGGG AGCTGAGTAG TCAGAGGTAA GGCCAGGCAG 960
GCTGCAGGCT CCAAACCCAC AAATGTTTCT AGTTTAGAGA TAGATGGATT GTCAGAAACT 1020
TGGAGGGGGA TTTCTAAAAG 1040