EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS026-02762 
Organism
Homo sapiens 
Tissue/cell
CNCC 
Coordinate
chr1:201871640-201874760 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2820315chr1201872264hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:201872202-201872220GGAAGAAAGGAAAGCAGC+6.3
EWSR1-FLI1MA0149.1chr1:201873313-201873331CCTTCTTTCTTTCTTTCC-6.56
RELAMA0107.1chr1:201872741-201872751GGAAATTCCC-6.02
ZNF263MA0528.1chr1:201872894-201872915CCCTCCCCTCTTCCTTCCTTT-6.19
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_01564chr1:201871239-201889995Aorta
SE_03068chr1:201871788-201872421Bladder
SE_03068chr1:201872679-201873369Bladder
SE_03068chr1:201873585-201873926Bladder
SE_03068chr1:201873962-201874599Bladder
SE_04721chr1:201874292-201875188Brain_Anterior_Caudate
SE_05468chr1:201871793-201873074Brain_Cingulate_Gyrus
SE_05468chr1:201873401-201875384Brain_Cingulate_Gyrus
SE_06244chr1:201871232-201876141Brain_Hippocampus_Middle
SE_26203chr1:201871299-201878534Duodenum_Smooth_Muscle
SE_26882chr1:201871768-201873424Esophagus
SE_26882chr1:201873515-201879304Esophagus
SE_38927chr1:201871616-201873452IMR90
SE_38927chr1:201873528-201876643IMR90
SE_46712chr1:201871827-201873343Ovary
SE_46712chr1:201873588-201875351Ovary
SE_48164chr1:201871344-201873481Psoas_Muscle
SE_48164chr1:201873508-201877499Psoas_Muscle
SE_48951chr1:201871608-201873470Right_Atrium
SE_48951chr1:201873519-201875935Right_Atrium
SE_50558chr1:201871748-201873414Sigmoid_Colon
SE_50558chr1:201873519-201878588Sigmoid_Colon
SE_51254chr1:201871229-201878188Skeletal_Muscle
SE_53198chr1:201871757-201873427Small_Intestine
SE_53198chr1:201873525-201876003Small_Intestine
SE_54511chr1:201871022-201890889Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1201872215201872821
chr1201873667201874226
Number: 1             
IDChromosomeStartEnd
GH01I201902chr1201871302201878377
Enhancer Sequence
CTTGACTCAT GGCAACCTCT GCCTCCCGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCTG 60
AGTAGCTGGG ATTACAGGTG CACACTACCA TGCCCAGCTA ATTTTTGTAT TTTTAGTAGA 120
GACAGGGTTT CACCATGTTG GTCAGGCTGG TCTCGAACTC CTGACCTCAT GATCCACCCA 180
CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCG CCGCGCCAGG CTGGGGGCTT 240
GAGTTTTATA CACAGCATAA GCCACCCACA CCTCCATGGA TCCCTGTTTC TTCCTCCGTA 300
AGGTTGCACC GAGCCTGAGC CCTGTTTTGA GAGCACTTGC TTCTCGTCTT CATCAGAGAA 360
GCAGAGGAAG TGGCAGAGTT AGACATTAGA CATAGAGTAG ACATTAGACT TAACTGTCCA 420
ACTGTGACCC CAGAGCAACT GGGACTTAAA GGGAGGCTGT GATGTCCTCC CCTAAAGGTT 480
TTTCAAGAGG AAGAGACTAT GGTTTGAATA TTTAAAAAGT TTTCTTTCAA GAGTGCCAGG 540
TTGGGGTGTG GGGAGAGGGC AGGGAAGAAA GGAAAGCAGC TCTCTGTCGC ACTCTCGGGC 600
CCAAGTAGCA TTTCTTCAAC CTCCGCTCTT CGCCGAGGGA ATGGAAAGAA AAGTGAGTCC 660
TATGGAAACG GTTTGTACCT GCACCACAAA CACATGCCAT TGGGGACCAG CCCCTGGGTT 720
TTTTTAGCAG CGAGAGTCCT TGGCTCCTCT GCTAGAATCA CAATAAGCAG CCAAGGGGCA 780
CAGGGCCTAG TGAGACAGGG CCTTGGAATG TATCTGTTCT AGCCTCCTGC CCTGCAGGCC 840
CCAAGGTCCA GCTGCACTGG AGGCCCCACT GGGGCTATGG TGATGGAGCA AGGGGCAGAG 900
AGCTCCCCCT CCCACTCACT CAGGCCCCCA GGGAACTGGG TTTGACCCTC AGATCAACTG 960
GGTTTGACCC TGGAGCAGAA GTGATGGTGA CCTTACTGAA CCTTGATTTG AAAGGGACAG 1020
AAGGAGAGGA GTATGCAAAT AGAATGGAAA CAAGGAAACC CAATGGATCA GCCCTTTTAG 1080
GATCTGCCCA TAGTTTGACC AGGAAATTCC CTCTCCTATT CCCTGATCCC ATCAAGTTGA 1140
GAGCAGTTCC ATCACTGATT CTGTCCACTT TTGGAGCTTG GAGGTGAGAG CTGGAGGGAC 1200
CAGCCTCTCT AGGCCCATGG TCTAGAGATT AGGCCTCCAG GGCAAAGACT CCTGCCCTCC 1260
CCTCTTCCTT CCTTTCCCAA AATGTGCACA TTTCAGGAGT TCTCAGAGCC CACTGTGCAC 1320
TGCATAGCTT CCCTTTCCAG AGTTCCCACG CCACTTGTAG GCTTCACTCA GAGAGAAACT 1380
GGGGATCCAG AGAGATGATG AGTTAACTGA CTTCACCTAG CAAGTTCGGG AAAAGCTGGA 1440
TTTCAGACCT GACTGTCTCA CTAACAGCCA CCAAGTCAAT GTAACCATCT CTAACCTTCC 1500
CCATCAGGGG CCAAAGCAGC TCCTCTCGGC CCACCCAGCA TCCCTGGAGT ACTCAAGTGC 1560
CCAGCTGCCC ACAGAGCCTC ACCCACCAGC CTCCTCTTTT CACGCAGCCC CCTTCAGAGC 1620
TAGGACTCCC ATTCAGACCC TTCCCTCTCA CCCCTAGCCA GGACTCAATT TAACCTTCTT 1680
TCTTTCTTTC CTTTTCTTTT CTTCTTTTTT TCTTTGAGAT GGAATTTCAC TGTTGTTGCC 1740
CAGGCTGGAG TGCAATGCCG CAATCTCGGC TCACTGCAAC CTCTGCCTTC TGAGTTCAAG 1800
CGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA GGCATGTGCC ACCATGCCTA 1860
GCTAATTTTG TATTTTTGGT AGAGACGGGG TTTCTCCATG TTGGTCAGGC TGGTCCCGAA 1920
CTCCTGACCT CAGGTGATCC ACCTGCCTCG GCCTCCCAAA GTGCTGTGAT TACAGGCGTG 1980
AGCCACCACG CCCAGCCTCA ATTTAACCTT CTTTCTTCCC TGACACCGCA CATCCTGACT 2040
TCTCCCCTTT ATCCTAATCC AGGACTACTC CCCACTCCTT CCTAGTTACC TCCCCTACCC 2100
TGGGGTCCTA GTTGGCAAGG ATCTGCCAAG TGTCTGTTCT TGAGGAGGTG TGCCAACACT 2160
TTAAAAAGAA CCTAATGAAA AACAGGCTGG GGGTGGGAGG GAAAGGGTTG ATTAATCATC 2220
AGTTTCCTCC AAATAGCCAG GAATGAGAGG GGCTGGAGCT TGTTGCCGCT TGTGTAGCCC 2280
TGAGCACTCA AACGTTGCCT TAAAAGGAGA AGGAGCCCAG AGTCCTCCCA GGGCTGGGAT 2340
TTCTGTTGAG CTGAGCTCCT CGGAGCCGGC ACATAGCAGA GCTGCTTCCT TCGTGCTAAT 2400
CTGAAAGGGA GGCTAGGAAA ACTTCTTCTT GCTTCCAGAA TTGATGGTAC ATCCCGGTGA 2460
CCTCCAGAGG TTATTTTTGC CTGTGTTTCT GTCGCTAGAC CTTACTCAAC TGTCTATCCC 2520
TTATAGCAGG AGGAATTTAG GTTAGATATA ACAAAGAACT TCCATGCAGT AAAGGTCCAC 2580
AGGCCTCTTG ATGAGAAAAC TAGGTAGCAA CAGTTATTTT TTCCCTTTGC GAAAAGCATT 2640
AGGGTTAGGG GAAGCCCGCA GGGGTGGTTT GGGAGTCCCT GGTTGGAGGC AGGGGAATGG 2700
AAAGGATGAC CTCTGAAAGC CGGTACTGAC CTGTGACACA TTGAGGTACC TAGTGATTGG 2760
GCTCAGAGTA AGAAACGGCT CCTTGCCCCC ATCTCCTCCA GGCCTTATGG CTACATGATG 2820
TTGCTCTGTG TCTGCCACGT GCGTTAGGAT CCAAGTTTAA TGCCTTTGAT AGGTTCAGAT 2880
GGGCAGAGCA CAGCATTTTC TCCCTTACCT TGGCCCTTCT GATGCTGCTT TCTTTAGAAG 2940
TCTTATCTGA TTAAACAGAG GAGAGAACAT TTCACCACCT CCATTGGCAA AAGATGAGAG 3000
GAAAAGGATT ATTTGTCTAT CCAGAAAGTT TAAAATGAGA ACTTGCTGAG AGCAAGGGCC 3060
AGAGCCTCTG TGTGCTGCAT TCGGCAACCA CAGCCCACTG ATACCTTGCC AGCCCACACC 3120