EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-15289 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr17:37909380-37912100 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2941522chr1737910368hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr17:37911206-37911219TGCAGCTGCCCCT+6.22
TFAP2AMA0003.3chr17:37910121-37910132TGCCTGAGGCG-6.62
ZNF263MA0528.1chr17:37911543-37911564TGAGGAGAGGAGAGAGAGGGA+6.06
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_10214chr17:37909224-37910777CD19_Primary
SE_10214chr17:37910780-37916505CD19_Primary
SE_10853chr17:37908831-37940013CD20
SE_11904chr17:37909311-37910613CD3
SE_11904chr17:37910792-37913737CD3
SE_14700chr17:37909278-37913385CD4_Memory_Primary_7pool
SE_15787chr17:37909511-37913218CD4_Memory_Primary_8pool
SE_16504chr17:37909204-37913320CD4_Naive_Primary_8pool
SE_17008chr17:37909810-37915266CD4p_CD225int_CD127p_Tmem
SE_17573chr17:37908953-37916175CD4p_CD25-_CD45RAp_Naive
SE_17896chr17:37909110-37915660CD4p_CD25-_CD45ROp_Memory
SE_18319chr17:37909158-37916527CD4p_CD25-_Il17-_PMAstim_Th
SE_19193chr17:37909271-37915605CD4p_CD25-_Il17p_PMAstim_Th17
SE_20202chr17:37909188-37916568CD56
SE_21224chr17:37909428-37913178CD8_Memory_7pool
SE_22122chr17:37909402-37915298CD8_Naive_8pool
SE_22381chr17:37908953-37916600CD8_primiary
SE_24275chr17:37909791-37912087Colon_Crypt_2
SE_25150chr17:37909728-37911614Colon_Crypt_3
SE_31091chr17:37909377-37915449Fetal_Thymus
SE_32555chr17:37909259-37916398GM12878
SE_33366chr17:37910098-37910578H1
SE_43567chr17:37909660-37915502MM1S
SE_47831chr17:37909909-37911257Pancreas
SE_50466chr17:37909230-37915264Sigmoid_Colon
SE_52845chr17:37909201-37915243Small_Intestine
SE_54478chr17:37909533-37913988Spleen
SE_55194chr17:37909333-37915072Thymus
SE_56927chr17:37909314-37909747VACO_400
SE_56927chr17:37909754-37911992VACO_400
SE_57786chr17:37909864-37911513VACO_503
SE_58042chr17:37909910-37911340VACO_9m
SE_58368chr17:37909481-37978016Ly1
SE_58889chr17:37909243-37979334Ly3
SE_60123chr17:37909329-37924165Ly4
SE_60580chr17:37909490-37957939DHL6
SE_60998chr17:37907678-37978969HBL1
SE_62252chr17:37909189-37978818Tonsil
SE_65636chr17:37909344-37912457Pancreatic_islets
SE_67296chr17:37909660-37915502MM1S
SE_69015chr17:37909810-37911434H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr173790980037910200
chr173790944337909600
chr173791041137911394
Number: 1             
IDChromosomeStartEnd
GH17I039753chr173790929737916397
Enhancer Sequence
ACTTGGATTA GGTTTATTTT AGGGTGGTTT GGGGCAGACT GAGGGAGATT GGAAGGCAGA 60
AACCACCCCC TCAGGACAAC CACGTGGATC TCCTTAGGGT CTGGGTAGTG GAACTGGGCC 120
CTGTGACCTT GGAGTTGGAG GGGAAGCTGT AAGCAGGGAT GGAACGGGCC ACCCGCACCC 180
TCACACAGCT GTGACCAACA GGCACGGTCA TCCGCATTCA CCTGCCCAAC TCCCATGCCC 240
TGAGTCCTGT CCTCCAGGGC ATTCCTACTG GCACTACCCC AATTTCCCAA AAGATTCCAG 300
GGATCTCTCT CTCGCTCTCT CTTTTTTTTT TTTTACAGTC TCACTCTGTT GCCCAGGCTG 360
GAGTGCAGTG GCTGATCTCA GCTCACTGCA ACCTCCACCC CCTGGGTTCA AGCGATTTTC 420
CTGCCTCAGC CTCTTGAGTA GTTTGGGATT ACAGGCGTGC GCCACCACGC CCAGCTAATT 480
TTTGTATTTT TAGTAGACGG GGTTTTGCCA TGTTGGCCAG ACTGATCTCA AACTCCTGAC 540
CTCAAGTGAT CCTCCCGCTT TGGCCTCCCA AGGGAGGGTT CCTTCCTCCC AGGCTGAGGC 600
ACCCTGCCCC ACACATCTAC TGGAGGAACT TAGTGTTGGG GCCAGGGGGT GGCTGGGTAA 660
GGCTGGATCC CACACTTGTC AGGCCAGGTT GGGGTAGGGG AGGATACACG GGGGACCCGT 720
CTCTCAGCCG TTCTGGGCCG GTGCCTGAGG CGATCTGCCC CGCCGCCCGC CCTTCCGCCA 780
CCACCCAAGT CGCATGCGCG CGCCGGGGCC GACGGGCGCC AGGCTCCACC GAGCCACCCT 840
CCGTCGTGGC GGCCCCTCGT GCCTCTGCGG AGGGAAGGCC GCCGGCTTCG CCAGGGGGCG 900
CGCGTCGGGG TCGCGGCTCT TTGAACTCGG CCCCACGAGG GGACGCGCCA TCGGTTTCGT 960
GGCTTGCGTG GCGCCGCAGC AACGAGCCGG TCGCCCCGGG GCGTTGCTTA GTCCGGGCCT 1020
CGCTGCGAGT CTGTGGGCGA GGCGGGAGGT GCTTCCTTGG CCAGGCGGGT GGAGGAAGGT 1080
GTGGGCGCCG CATCCCAGCG TCGCGGAGCC TCCAGGCGCG GGCAGGCGAG ACTGGCGTGC 1140
AGCGCGACGG CCTAGTCCCG GCGTCCCACC GTCCCCCACT CCCGCAGGCG CCGAGCCGAT 1200
TCAGCCGCGC GGCTGCAGTG ACACCCAGCG GCCGTCGCGG GAAGTGCGGT CGCCGCGGCC 1260
AGGCCTCCGG GGCTCCTGTC TCTCGAGGTT CCCACCCCGG TTACGCGCGG GCACCCCGGA 1320
GGAGAGCGGC CGCGCGCTGC AGATGCCCGC GGGGGCACTT CCCCTGCCCC TCCCCCGTTT 1380
CCTCCCCGCA GGCGCCCGAG CGCCGGGAGA TCCTGCGCAG CGGCAGTGCC CGGAAGGGCG 1440
GGGCGGGGTG CAGCAGCGGC GCTGGGCTGT GACCCGGGCA GTTTCACTTC TGGATCCTGC 1500
TCGGGCTGTG ATAGGACAGC GCGGGGGCAG CGGGGGAACA CGCGGGCACG CCGAGATCCG 1560
GCGCTCGGGA CCCCGATGAG GGGAGGCCTT TCACTCCTGG GGTGTCACGC GACCCACGCT 1620
TTCCTCCATG TCCACTCCCA CCCCCCATGG GTTCCACTTT GCTGTCCCCC GAGCTGCCGC 1680
TCCTCCCCAG CAGACACCGT CTCCGCCGGG GCTGCCGACC CCCGGAGAGG CCCCGAGCGG 1740
CGTGGGCGGC GGGAGGAGGG AGCTGTGAAG CCGCAGGCAG GGGGTTAGGC TGCGGGCTGC 1800
TGAGACGCCG AGCTGTTTCT CAGAAGTGCA GCTGCCCCTC CCCTCACACC CCCCTCACTC 1860
CCACCGCGCG CCGCACCCCT GCCCCCTCTC CGCCGGCCTC CCTTTCCTCT CCCAGGCACC 1920
CTAGCCGGGA ATCTGGGGTC TGGGTCCACG CAGAATTAAG AGGAGAACCT GAGAAAGGGC 1980
GGGGGCCGGG GGTTCAGACC CAGCCTCAGC GCGCGTTATT CCGAGCCTCC TATAATTCCA 2040
CAGGTGAGGG GATCCTGTCC CCTACCCCTG GGGTCCAGGA TTGGAATTTG ATAGAACAGT 2100
TAGGAAAATG ACATCTTGAG AGAGTCAGGG CCCGGCCACT ATTACTCTAG CTCCAGCGTC 2160
CAGTGAGGAG AGGAGAGAGA GGGAAGACCT GGAGCCCGGC TGGTGCAGTG AGGTTGAGGC 2220
CTGTCTTAGG AGTACCAGCT GGAAGGCCCT TCAGAGATCC CTGACTCTGG GGAAAATCAA 2280
CGCCCAGAAG GGGAAGTCAA GTGTCTGGGC TCATCCCGAG AGGGAGAGGG CTGGGATTGG 2340
AACCAGGACT CCAAATAGTT GCGGGAGTCT GCGACTGTCT TTTGCTTGGG ACTTCAGAGC 2400
TTTGCTGGAT TCACTGACTC AGCCTGCTTT CCCTCAACAC ACACAAACAC ACACACACGA 2460
GACACGTGCA CGCGCGCACA CACACAGATA CACAGACACA CACAGACAGA CATGCAAGGA 2520
GAGAGACAGG CACACATGGA GACAGACACG CACACGCAAA GAGACACACA GCTCCCCAGG 2580
AGTCTAGCGG GGCAGCTGAG GTCTGTGAGT GAGACATTCT CAGTGAGACA CTGAGAATGC 2640
AATTCCAGTG GGGGTGGGAT GGGGATTGGG CGGTGGAAGG ACAAGCCCGG GGGAGGAGGT 2700
GGCATCGCCC CCCTAGTTCC 2720