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

TagContent
EnhancerAtlas ID
HS133-13695 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr17:79023250-79025120 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs8067235chr1779024637hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TFAP2AMA0003.3chr17:79023912-79023923TGCCTGAGGCA-6.02
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_25200chr17:79022511-79025155Colon_Crypt_3
SE_26560chr17:79022179-79025369Esophagus
SE_31420chr17:79022257-79025350Gastric
SE_34261chr17:79015484-79025415HCT-116
SE_36440chr17:79022176-79025537HMEC
SE_41709chr17:79023438-79025169LNCaP
SE_42160chr17:79015988-79025385Lung
SE_47416chr17:79021645-79027438Panc1
SE_47964chr17:79023284-79024545Pancreas
SE_57453chr17:79022161-79025209VACO_503
SE_65309chr17:79022165-79025391Pancreatic_islets
SE_69007chr17:79022537-79023808H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177902418779024380
Number: 1             
IDChromosomeStartEnd
GH17I081048chr177902218879027464
Enhancer Sequence
CTAGGTTTTT CTGGGTTTTT TGCACCTCTT GGTGTTGATA AGAAACAAGC TCCCTTCCCC 60
TTTTAAAGCC CACAGACTTT CCCGATCTCC TCCCCATCCC CTGCCCCAGC ACTGTCAGGG 120
CGTCTGGGCG TCTGAGCTCA GCTCCTTCCT GGTGGCATCC TGCAAAAAGA TACACTCGCT 180
CAGTGACTCG GAAAAGCCAC GTCGGTGTGG CTGAGAACAG AGTTCTTTCC ACCTGGGGCC 240
GCTGCTGTTG GTTTTCATTC CGGAAGAGCT GGAGCTGCCT GTCACTGGCT CCCCTGCCCC 300
CACCTGGGGA CCCCCAGGCA CTGCAAAGTG CCTGTTGGCT ATGGGCCCCC GGACCAGGAC 360
CTTGGCCTGA TTAGGGGAGC CGGAGGTGGA AGTGGAGGCG GGACTGGAGT GTATGCCCCA 420
CAGTGGGCTC TCCTCAGGCT GGGGACTTCC ACACGGGCCC ACTGGGTCAG GATGGCCCGT 480
GCCTGTGTTC TAGGATAATG GGATGGACTG GTTCGGAGGC TCAGAGAGAC GCCTGACCAG 540
ACGCCTGACT GGAGATGGTC TCCCAGCAGA GGGGCTGGGC TCTTCAGGGG CCACTGGGCT 600
CCTCCCGTGG TTCCTGGGAG AGGGAGGAAC CCGGAGGAGG GGTGGGTGGC ACCTACAGTG 660
CGTGCCTGAG GCAGGGCTCC ACAGAAGGCC TCTCTGCTGG CCCAGCGGCT GGATGCAGAT 720
GCAGAAGGAG GAACTGGCCC TTCCGCCCGC CCGGGAAGGG GAGTCCCCCC TTACAATGTT 780
GGCTCAGTGG GATCGATGCC TCTGCCATTG CCTTCGGGCC AGGACAGCAG CACTTGCGTG 840
TCCCGGCCGC CGCCCCTCTC TTGCAGATGG AGGCAGGGCC GTGCCCAGGT GTCCTGGTGG 900
CTGTTCCCTG CCCGCTGTCT CCTGCATTCC TTCCGTGTGA GCTCAGCTGC TGCACTAAGG 960
AAGCGAAACC TTGGTGCTGC CCCGTGCGTC ATGCGGTAGG CATGGCCGCC GTGCTGACCC 1020
GCCGTGGTTG GCCCTGGGTG GCTCCTGGCC TGTTTCTCCT GCTGCTCAGG ATGTTAGTGG 1080
AGCTCACAGG GCTCAGGTTG AGCCTCTTCC ACCCGGGGGC CTGTGGGGGT CATGGTCCTG 1140
GAGCCAAGCG CGTGGGGCTC TTGTGAGCAA GGGGTCTGCT CTGGCACGCC CACCTCCGTG 1200
GTAGTGTTTT CATACCTGTG TCACACAGGG TGAGAAACAT GCTTGATGCT GCAGCTCAGC 1260
ACACACACGC ACACAAATGT GCACATGCAC ACGTGGACAC ACATGCACAC ATGCATGTGT 1320
GTATGCACAC ATGGGCACAG ATGTGCATGC AGACATGAGC ACACGCACAC CAGAACACTA 1380
GAGTCGGCCG CATCCTCCTC ACTTGGCTGA TGCCCCCTTC TGCTTGATTT CATCACAAGA 1440
AACGCGCATC CGGCAGCATT TCCCGACCGC CTTCACCGCC AGTCCCGGTC TGCATGGTCA 1500
GTTTGAACCA GGCTGCCGAG AGCGCACCAG GTCCCAGCAT TCTCCTCTCT GCTGGTAACT 1560
CTTCAGGCAT TGTCTCTGGC TCACGTTCTC CTGGGCGCCA GACCTATCTC ACCCCACTCC 1620
CGGTGTGGCC TCCCTGCCCC GGCTCCCAGG CACTCCTGGG AGTTAAAGTG TCCAGGCTCC 1680
TGGTTCATTG CTGAGTGTTT AGCTCAGTGC TAACGCTGCT GTGCTCCAGC ATCCCCGTCC 1740
CTTTAGGACA GAGGCCTGCG TGGTACGTGC CTCTCTGCTC CAGCATCCCC GTCCCTTTAG 1800
ATCAGAGGCC TGCGTAGCAC ATGCCTCTCT TCCCCTCTGA CATCCCAGAG CCTCTGATGG 1860
GTCTCCCAGC 1870