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

TagContent
EnhancerAtlas ID
HS108-14642 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr16:11489450-11493060 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12596613chr1611491007hg19
TF binding sites/motifs
Number: 27             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr16:11490252-11490271TAGCCACTAGATGGCGGGG+6.74
ESR2MA0258.2chr16:11492211-11492226AGGTCACAGAGCCCC+6.14
EWSR1-FLI1MA0149.1chr16:11491602-11491620GGAGGGAGGGATGGAGGG+6.03
EWSR1-FLI1MA0149.1chr16:11491618-11491636GGAGGGAGGGATGGAGGG+6.03
EWSR1-FLI1MA0149.1chr16:11491630-11491648GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr16:11491634-11491652GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr16:11491638-11491656GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr16:11491753-11491771GGAAGATAGGAAGGAGGA+6.22
EWSR1-FLI1MA0149.1chr16:11491749-11491767GGATGGAAGATAGGAAGG+6.54
HES2MA0616.2chr16:11491272-11491282GGCACGTGCC+6.02
HES2MA0616.2chr16:11491272-11491282GGCACGTGCC-6.02
MEF2AMA0052.3chr16:11491302-11491314TCTATTTTTAGT-6.27
MEF2BMA0660.1chr16:11491302-11491314TCTATTTTTAGT-6.32
MEF2CMA0497.1chr16:11491301-11491316TTCTATTTTTAGTAG-6.57
ZNF263MA0528.1chr16:11491695-11491716GGAGGATGAATGGATGGAGAG+6.23
ZNF263MA0528.1chr16:11491595-11491616GATGGAGGGAGGGAGGGATGG+6.25
ZNF263MA0528.1chr16:11491611-11491632GATGGAGGGAGGGAGGGATGG+6.25
ZNF263MA0528.1chr16:11491639-11491660GAGGGAGGGAGGGAGGGATGG+6.63
ZNF263MA0528.1chr16:11491607-11491628GAGGGATGGAGGGAGGGAGGG+6.82
ZNF263MA0528.1chr16:11491623-11491644GAGGGATGGAGGGAGGGAGGG+6.82
ZNF263MA0528.1chr16:11491603-11491624GAGGGAGGGATGGAGGGAGGG+6.92
ZNF263MA0528.1chr16:11491619-11491640GAGGGAGGGATGGAGGGAGGG+6.92
ZNF263MA0528.1chr16:11491599-11491620GAGGGAGGGAGGGATGGAGGG+7.29
ZNF263MA0528.1chr16:11491615-11491636GAGGGAGGGAGGGATGGAGGG+7.29
ZNF263MA0528.1chr16:11491627-11491648GATGGAGGGAGGGAGGGAGGG+7.5
ZNF263MA0528.1chr16:11491631-11491652GAGGGAGGGAGGGAGGGAGGG+7.97
ZNF263MA0528.1chr16:11491635-11491656GAGGGAGGGAGGGAGGGAGGG+7.97
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr161149042711491200
chr161148975411489870
chr161148997511490921
chr161149190911491992
Number: 1             
IDChromosomeStartEnd
GH16I011395chr161148976111491038
Enhancer Sequence
ATGCCGGGAA GGGAGGGAAC TCCCCTCTCA CAAGCACCTG CTACATGCAG ATGTTGTACA 60
AATGTGTTTG CTCCTAACCA TTCTGCAAGG GAGATGGTAT TTGTTCCCAT TTGACAGAGG 120
GGAAGACTGA GGCTCAGCAA ACGAAAGTCA CGAGGCCAAG TTCACCTGGC CAGGGAGACA 180
GAGGAGGTGG ATGGAAACGC CGAGAGAGCA CCTGCTACGT CACGTGCCTT GGCTACGCAG 240
GCAGCGGGAA CCGGTATCCA GACTCCCAAA AACCACCCTG TGAAATATCT GATCCCCTCC 300
TACAGATGAG GAAACACATG CTCAGAGAGG TTCCTTCCTG GGATCACCTG GCCAGGTCAG 360
GGCAGAGTAG GTATTGGAGG CCAACTCTGC CCCTTCCTAC TTCCCAGGGC TGCTGGGAGT 420
AAGGAGGGGG AGGAGATGGT ACCAGTAATG GCTAATAGCA AATACTTACG TAGTGGCTGT 480
TTTCTCTCAG GCACTGCTCT AAGCGATCTA TGCCTACGAC TATATTTAAC CCTTGCAATA 540
TTAACCCCAT GGGAGATAGG GCCAGTACAA TTATACCCAT TTTACAGGGG AGGAAACTCA 600
GGTACCAGGA GGCAGCTAGG CTGGGATTCA AACTTGGGCA GCCCAGCCAC TGCCTCTCTG 660
TTATAGGAAG GGCCGGGTGT TGGGACTGTG GAGGAGCTGC CTTGTCTTGG CGCCAGGGCC 720
AGGCCTGGGG TTCAGCAGGC GTTCCCCCGA CCCAGAATGA AGCTCTGGCC CCATCCAGAA 780
TGCTGGTTTG CAGTTCCTCA GATAGCCACT AGATGGCGGG GCCGCCCAGG CAGTTGGGGG 840
CCTGCTGGCC AGGGAGGAAC CGCAGGGATG CCGGGATATC TTTCCCAGGG ACTGTCAGCC 900
CCATCCTGGC CACTGACCTC CAGTGCCCCG GAGAAGTCAG CTGAACGAGG CCTGCTGTGG 960
TTTTGGAGGG TCAGGCTGAG ATGCAGGCCG TGGTCTGGGT CTGGTGCAAG GCCCAGGTGG 1020
CAGCGGGAAC GCAGCAGGAG TCCACCCTGG CCCAGGGTGT GCTCCCCGAC GACCAAGAGG 1080
GCCTGGGACG AGAGAGTCTA GGTGTCAGGC AGGCACAGGG GTGGCAGCTT CCTCTCTCCC 1140
CAGTCCCCTG CACCGAGAAT GCAGCAGCAG CTGCCACCTC CCAGCCTCCA CACCTGTCGC 1200
AGCTCACAGC TGACCTCTAA GAAACGCAAA TCAGATGCCG TCCCCTAAGA AGCTGGGCTC 1260
TGGCATGGCC CGTGGCCTGC TTTGTTGTCC CAACCTCACT TCCCTTGCTC CCTCCGTAAG 1320
TGCTGCCCCG TGTTCCTCAA GGCAGAGTTG TGCCTTAGGC CCCTTCCCTC TGCAGGGCTC 1380
ACACTCACCA GTGAGGCCCC TTTTTGCAAC ACCCTGGCCC CTCTCTGCTT CATTCCTGCA 1440
CAACGTTTAC TACACCCTGA CCATAGACCA TGCATCTCTA GTTTGTTGTA TCGTCCTGGC 1500
CCCACTGGAA TGCGCCACCC AGGAGGCCGG CACCTAGGCT GTGTCTTTCA CATCCACTCC 1560
CTGCACCTAG AACACAGCCT GGCATAGGTG AAACACACAA ATGTTTTCTG AATGAACAGA 1620
GGAAAAGATA AGGGGTGGGA AACTATGGTT TGGGGCCGAA TCTGGCTCAC TGCCCACTCT 1680
TGTAAATGCT TTTTATTTTG AGACAGAGTT ATGCTCTGTC GCCAGGCTGG AGTACAATGG 1740
CACGATCTCA GCTCACTGCA ACCTCCGCCT CCCAGGTTCA AGCGATTCTC CTACCTCAGC 1800
CTCCTGAGTA GCTAGGACTA CAGGCACGTG CCACCGTGCC CAGCTCATTT TTTCTATTTT 1860
TAGTAGAGAA GAGGTTTCAC CATGTTAGCC AGGATGGTCT CGATCTCCTG ACCTCGTGAT 1920
CTGCCTGCAT CGGCCTCCCA AAGTGGTGGG ATTACAGGCG TGAGCCACCG CACCCGGCTT 1980
GTAAATACTT TTACTGGAAT ACAGCCGTAA GGATTCATTT ACATATTGTC TATAGCTGCT 2040
TTCACAAGAC AGTGGTAAAG TTGGTTGTTG GAACAGAGAC TGGATGGTTC ATAAAGCCTA 2100
AAATATATGC TATCTGTCTC TTTACAGAAG AGTATGAGTC CTTGGGATGG AGGGAGGGAG 2160
GGATGGAGGG AGGGAGGGAT GGAGGGAGGG AGGGAGGGAG GGAGGGATGG ACGGACGGAT 2220
GAATGGATGC AAGGGAGGAA CGGTTGGAGG ATGAATGGAT GGAGAGAGAG GGTACATGGG 2280
AGGGCAGATA TACGGGGATG GATGGAAGAT AGGAAGGAGG ATGGAAGGAT GCGTAAAGGA 2340
ATGGATGGAT GGGTTGGTGG ATGGAAGAAC CAATCAACCA GCTACCAACC CCAGGAGGGG 2400
AAAGGGGTTG AGGAAAAGGA GTCCTAACAC CTCTCCTCTG GGGTAATGAT GACTACAGCA 2460
GCTCTAACTC ATGTGCCCGG CACCAAGGCT GAGCATTCCC GCATCATGTC TCTCTTAAGT 2520
CTCACCATCA CTCTACGTCC TGGAACCTGC TGCTCCTTCC TCAGATGAAA CACCAGAGGC 2580
TCAGAGAGGA GATGTGCACT GCCCAGTCAC CCAGCAGGCA AATGGCAGAG CCACGATGGT 2640
GGCGTCTGGC TGCCTCGCTC ACACCCCTGC ATTCTGCGGG CACCACCCTC ACTGCTGCCC 2700
CCTCACCATG GGTCCCTGGT CCTCCAGCTG CCCCCTTCTG CAGGGCAGAC TCACCCTGGG 2760
CAGGTCACAG AGCCCCAGGT GGAGGGAGTG CCGCAGCCAG CGTGCATAGT CAGTCTGTAC 2820
TTCTCCCCAG AAGCTCTGAC GGGTACAAGA GGCCCCGAGG ACGTGCTCCA GCGTGGCCTC 2880
CATGATGATC TTGTCTGGCT GAGATGGCCA ATGCCTCTGG AATGAGAGGG CCTATGGGTC 2940
AGGGGCTCAT CACCTAAGAG AATGCCCATG GCCAGCTGCA GTTGGAGACC CTCACCTAGG 3000
CAAGAGCATG TGCCAGGAAT GTGCCGTCAG AGCTCTCATC AGCCACAGCA CCCCCTTACA 3060
CTCTGCGGCA GGATTTTTTT TTTTTTGAGA CACTCTTGCT CTATAGCCCA GGCTGGAGTA 3120
CAGTGGCATG ATCTAGACTC ACTGCAACCT CTACCTCCCA GGTTCAAGCG ATTCTCCCAC 3180
CTCAGCCTCC CAAATAGCTA GGATTACAGG TGCATGCCAC CACGCCCAGT TTTTTTTTTA 3240
ATTCTTTAGT AGAGATGGGG TTTCGCCATG TTGGCCAGGC GATCAGGTGA TCCCCCCACC 3300
TCAGCCTTCC AAAGTGCTGG GATTACAGGT GTGATTCGCC ATGCCCCGCT CGTGGCAGGA 3360
TTTCTGCTGT GAGCACTTAG GGGGCCATGC CTAAGAGCCC CAGGAACCCA GGCGGGAGGT 3420
CCAGAGGAGG AAGGGGCTTC CAGGGCCAGC TCTCCCCATT TCTCCATGGC CTGGTTCCTG 3480
CCCCAAGCTC TGCAGAACAG TGCTCGGCCC CATGAGGAGC CCTATCAGGT AATGATGCTG 3540
GAGGAGACCA GACCTGATGC CTCGGGGAAC CGGAGCTCCC GATCTCCCTC CGCCCCCTCC 3600
CGAGAAGCCC 3610