EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-11875 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr15:67466370-67469700 
SNPs
Number: 5             
IDChromosomePositionGenome Version
rs12912010chr1567467143hg19
rs12912045chr1567467297hg19
rs12913547chr1567467507hg19
rs17294280chr1567468285hg19
rs35251008chr1567468525hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HES2MA0616.2chr15:67469246-67469256GGCACGTGCC+6.02
HES2MA0616.2chr15:67469246-67469256GGCACGTGCC-6.02
RELAMA0107.1chr15:67467407-67467417GGGAATTTCC+6.02
TBX21MA0690.1chr15:67467969-67467979AAGGTGTGAA+6.02
TBX2MA0688.1chr15:67467969-67467980AAGGTGTGAAT+6.02
ZNF263MA0528.1chr15:67467455-67467476GAAGGAGGAGGCAGGTGGAGA+6.44
ZNF263MA0528.1chr15:67467458-67467479GGAGGAGGCAGGTGGAGAGAG+6.66
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_09181chr15:67466836-67470715CD14
SE_10875chr15:67463174-67471168CD20
SE_18371chr15:67463340-67469893CD4p_CD25-_Il17-_PMAstim_Th
SE_23212chr15:67466304-67468217Colon_Crypt_1
SE_26536chr15:67466309-67469672Esophagus
SE_31411chr15:67466416-67469347Gastric
SE_37787chr15:67466568-67472740HSMMtube
SE_37941chr15:67465373-67472958HUVEC
SE_38928chr15:67462159-67469899IMR90
SE_42172chr15:67467092-67469654Lung
SE_44471chr15:67467419-67472425NHDF-Ad
SE_44749chr15:67466055-67469674NHLF
SE_45534chr15:67453126-67473814Osteoblasts
SE_47100chr15:67357928-67475420Panc1
SE_48052chr15:67464183-67473310Psoas_Muscle
SE_50064chr15:67466721-67469446Sigmoid_Colon
SE_51081chr15:67466500-67469701Skeletal_Muscle
SE_51874chr15:67467444-67469444Skeletal_Muscle_Myoblast
SE_52344chr15:67466124-67469783Small_Intestine
SE_63662chr15:67467303-67469755HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr156746653667466604
chr156746698067467913
chr156746817167468380
Number: 1             
IDChromosomeStartEnd
GH15I067171chr156746362167474069
Enhancer Sequence
TTTGGAAACC ATGAACACAT GTGGCAGCCT TTCCCATAGC GGGGCCTGAG AGAAGGGGTT 60
TGGTGGTTGA ATGAGTGTGG AAAGCCTGTA TTGTGGCCTC TCCTCCAGCC CCCACTCAGG 120
AGGGACTCAC ATGGCCACGC TCTGAGGAGC CTGCAGAAGG AGGCCTGTCT GACCCAGCCT 180
TCCTCCCATG CACTGATCAC TGTTCCTGTA CTTCTGTCTT ACCGCCCCAT TACCCATCCA 240
TAGATCTGAC TCTGGAAACA CCGATGAAGT TTGGCTGAAG TCATGCCAGT GGATGGATTT 300
AGTGGAGAGG CCGACCCAGC TCAAGATGGA AAGACAGCCA GAGATGCGCT CGGGTGGTGG 360
GGGTTCCTTG GAGAAGGCTG AGGTCAGGGG GATGATGGGG TCACAGCAGC TCAGAGGGGA 420
GGCAAGCCCT GAAGGACAGT GGCTACAAGC GGGCCCTGCA GAGATGCAAA ATGAGATTTA 480
AGAAGAGGCC TTGGATTTGG CATCAGGGTT TCAAGGGGGA GCTTTTAGGG AGCAGTGTGT 540
AGGAGGGGAG GGGCTGCAGT CAGTCAGCAG TGCACTGAAG GGCAAGTACC AGGTGGGGAG 600
GTGGAGGCAC CCAGCAGCGC AGCCTTTGTG CTGACTCACA GTCAGTGCGT CCCAAACCCT 660
AGGATGGAGG CAAGCACACA GGGAGCTCTT CCTAGGAAAA AATGGGGACA TCTCAGGACA 720
TCTGATTATT TCCTTTAAAG AGATTATTAT GAAATTACTG TACAAAAAGA AAGAAAGCAG 780
AGGACATCTG GTTTCTCCTT TCATTTCCTC CCCACTCCAG GTGTTAGCCC CAGGGCTCAG 840
GTCTGGGGAA GGTTGAGCCT CCTTGCCCCA GCAAAGCCAC TTCTGGTAAG GGGCAGGGAC 900
TCCTGGTTGA GACCTGGCTC AGCATCCTGC CCCAGGCAGG CTCTCGGAGA CCCTGGGACC 960
TGGGACCGTT GTTTGCAGGG CAGGAGATAT GAGCAGGTGA TGTTCCTGTT ATTACACAGC 1020
GTGCTGGGTG AGTCACCGGG AATTTCCTAG GCATTTAAGG CGGAAGGATT GGGGTAAATG 1080
GAGGGGAAGG AGGAGGCAGG TGGAGAGAGG AAAAAGGTAG TGAGCTGGCT TCTGCCTGGT 1140
GAGTAAGTTG TTCCCTGCTT TAAAGTGAGA TGATTAGGGC GGAGCCATGA CTGAGGAAAA 1200
TAATGTACCA GGGAGAGCCC TGAGGGAGCA GTTGAGCTGG AGTTAAAGGA GGTGATGGCT 1260
TCCAGAGTGC CAGTGGCAGG AGTGAGAGGC AGGGATGGGG CAGCTTGGAG TGAGAGGGAT 1320
AGGGCAGCTT GGAGGTGGCT GATGCCGGAT GCAGTGCTTC AGACTGAAAG GTGGTCGTTT 1380
GCTGTGAATT GCCCTCTAGA TTGTGTAGAC TAGGATGATG GGATGTTTCT TGAGCTTGGA 1440
CCCAAGGCAG CATCTCCTGT TGACATAGTT CTCCCTCCCT ACTGACGCTT CCTCAGGCAC 1500
CTTGCCTGAG AGTTGAGAAT TCTTAGGTTA TTTCTTCCAA AGGGAGGACC CTCCCCCCAG 1560
GGTGCCACTT TGCACTGGCC TAGTTGCACC TCTGCTGGGA AGGTGTGAAT CGGGGGCAAG 1620
TTGCCCCGTG AGTCAGGGTT AGGATTCTGG GTGAGACTCC ACGCTGACAG GCCCGGCTTC 1680
CCCTCTGCTT CATGAGCCCC TGTGCCCATG TGTGAGCACA GGTGTGGTGG CAGGGCGGCC 1740
CGAAGACCAC CAGCCCTGAG TGTGGACGGC GGCCCAGGGC AGAGGCCCAA CCCAGTTCCA 1800
GGCATCTTCA TGCTGCTGCC CAAGGCTCTT TTACAATGCA GCCTCTGGCT CCGGTCTTCC 1860
CCACACTTGT GAAATCACAG GCAGGGTCTT CCCCACACTT GTGAAATCAC AGGCAGGCAA 1920
CATAATGACA GGAAGTCAGC TGTCGGCTCT GTCTTCATAC TCCTGAGGGC CCGGTTTTTA 1980
GACTTTGCCA CTGTTCCTGG TTGCAGTATG CTGGTCATAA GCTAAAAGGG CATGGGGGTC 2040
TCTGTGCAGC TTGGTTTGGT ATTTTAGTCC GCAGATACAT AGGTTGGAAT TAGTACCCTG 2100
GGTGCTGGGA CACAGCTGGC GTGGGCTCAC AGAGACCTCA TCCTCTAGCA TAGGAGACTC 2160
AGGTACACAG TTTCTGGGAC ACAAGGTTAA TTCTGCACTG AGGCAGTGAG GGAGTGTTTC 2220
ACAGCCGTGT GAGCTGGGCC TTAAAGATCG AGTCCCTGCA GAGGAGGGGG ATGGGCAGTC 2280
CAGGCAGAGG ACCCAGGCAG GACTGAGAAG TGGTGGATGA GGAACATGGG AACTGGAGTG 2340
TGGAATCTCC TAGATTGAGG AAGAGCTGCC TTCCGCAGGT GAGGTGGGCC CAGCAGAAAC 2400
CAGCCCATTT CTGTTTTGAC CTTTCGTCTT GCAGCAGCAG TGCTCCTGGC CTTTGCCCGT 2460
TCCTTGCTTT CGATTTATAG GAGAAAGTTA ATTTCCCCCC TTGCCTCCCC ACCTCTTCCT 2520
TTACGGGATT TGAATCTCTT GCACATGTTT TTAATAGGCA TCCCTTAATC CAAGTGTTGC 2580
CTTCTGGGTT TTATTCTGTT TTCTTTTTCT TAAACATAAT GGAACGTCTG TGCCAGCTTG 2640
GAACAGGACT GAAAACTGAG GCCAGCCAAT GCGTTAGGCT GGCAGGGGGC CAGCCATGGA 2700
TTAAGTGCCC TATGGCACTT GAGAAGTCTG GCCGACACCA CACTGGTGGG GGAGGGGGAT 2760
CCACAAAGGC TGGAGCTGGA GGTTCCTGCG TCTCCAACAC CTCTGCACTG GGAGGAGAGA 2820
TTAGCACAGA CTCAGAAATC TGGCCAGGAG CAGGGCTGTT TGAAGGGAAG GCCGTGGGCA 2880
CGTGCCATCG TCTACCACCC CAGCTGTGCA AAATGCTCAG CCTAGAGGTG AAACTGCTCT 2940
TCAATGGGGT GTGTCACCTT ACCCCCCGTA GTCATTCTCC TAGAGGAGCC TTCTATAGAA 3000
CTGCTTCTGC ATTTGTTGGT AAATCCTTGA AACCAGATCT TAATTTGCTT GCTTGCTTGA 3060
TCAGTTGATT GATTGGTCAG GGGAGGGGTT GCCACCTCCC CCTGAGAGAT TTCTTTTAAG 3120
ATTTAATGCC AGGACAAACT TTGTTTTCCC TGAGGAACTA GTAAGCATTG CCCATCCACC 3180
AACCAGAGCC ATAGACCATG TCATGTTCCC TTTTTGTCTT GTCTACTAGG AAGCTCAGAG 3240
CCAAACTGGA TGCTTTTGCA GTAACTATAA CCTCATGGTT ATCCCATTTA TAGCCGCCTT 3300
CTTTCCAGAG TCCTTTTTGT TTCTCTGGTA 3330