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

TagContent
EnhancerAtlas ID
HS098-36105 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr21:45150530-45153940 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs142471995chr2145153706hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXH1MA0479.1chr21:45152579-45152590TGTGGATTCGG-6.02
ZNF263MA0528.1chr21:45153130-45153151CCCACCCCCCCCCCCGCCCCC-6.14
ZNF263MA0528.1chr21:45153404-45153425CCCTCACCCTCTCCCTCCCTC-7.4
ZNF740MA0753.2chr21:45153131-45153144CCACCCCCCCCCC+6.44
ZNF740MA0753.2chr21:45153143-45153156CCGCCCCCCCCGC+6
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00247chr21:45144991-45153132Adipose_Nuclei
SE_00247chr21:45153136-45157947Adipose_Nuclei
SE_01223chr21:45151058-45152340Adrenal_Gland
SE_04683chr21:45150848-45152643Brain_Anterior_Caudate
SE_04683chr21:45153147-45155820Brain_Anterior_Caudate
SE_23454chr21:45150874-45152392Colon_Crypt_1
SE_23454chr21:45153130-45155185Colon_Crypt_1
SE_23996chr21:45151210-45151631Colon_Crypt_2
SE_23996chr21:45151648-45152097Colon_Crypt_2
SE_23996chr21:45153137-45155164Colon_Crypt_2
SE_24783chr21:45151042-45152404Colon_Crypt_3
SE_24783chr21:45152993-45156528Colon_Crypt_3
SE_27346chr21:45151427-45155322Esophagus
SE_27888chr21:45146658-45155080Fetal_Intestine
SE_28755chr21:45146573-45155040Fetal_Intestine_Large
SE_32085chr21:45151054-45152438Gastric
SE_32085chr21:45153093-45155352Gastric
SE_41875chr21:45153129-45154741LNCaP
SE_42672chr21:45153163-45156266Lung
SE_53011chr21:45150192-45152538Small_Intestine
SE_53011chr21:45152957-45155160Small_Intestine
SE_57364chr21:45153463-45155047VACO_503
SE_57997chr21:45151228-45152061VACO_9m
SE_65700chr21:45151166-45152439Pancreatic_islets
SE_65700chr21:45152924-45155098Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr214515097345152712
Enhancer Sequence
TACTTTTAAT ATAGTTTATG TAGTCTGGGT GCAGTGGCTC ATACCTGTAG TCCCAGCACT 60
TTGGGAGGCT AAGGGAGGAG AATTGATTGA GCTTAGGAGT TCAGGACTAG CCTGGACAAC 120
ATAGTGAGAC TCTGTCTCAA CAAAAAAATA TAAAAATTAG CCAGGTGTGG CAGCACGCAC 180
CTGTAGTCCT AGCTACTCAG GAGGCTGAAG AGGGTGGATC CCTTGATCCC AGGAGTTCAA 240
GGCTGTAGTG AGCTATGATT GTGCCACTGC ACTCCAGCCT GGGTGATAGA GTGAGACCCT 300
GTCTCAAAAA ATAATAATAT AATTTACATA ATTGTAAGTT TTATGACTCA ATTTTTTTTT 360
TAAATAGAGA TGGAATCTTG CTATGTTGCT CAGTCTGGTC TTGAACTCCT GGGCTTAAGT 420
GATCAATCCT CCAGCCTCAG CCTCCCAAAG TGCTGCGATC ACAGGTGTGA GCCACTGTGC 480
CTGGCCATAT GACTCAGTTT TTAATAATGA CTCTACGTAA AACTGACCTG CACTATTGCA 540
TCTGGCAATC GCGTGGCCCA ATCCATCTTC AAAGCCAGCA ACAGTCGTTG AGTCCTTCTT 600
TTAACTTCCA ATCTCTGATT TTTCCTTCTG CCCTTCAGCC TGAGAAAACT CTGCTTTTGA 660
AGGGCTCATG TCATTCAATT AAACTCTCCT GGATAAGAAG ATCCTCATGG GAGAGAGATC 720
TCATCACACT GACAGGTTTC ACCCACACTC AGGGGGTTGC CCGAGGGTGA GCGGGGTCCC 780
TGAAGGTCAT TCTTAGAATT CTGCCACGGA AGAGCCCCAT AGGCCATTAT AGGGACAGGG 840
TTTACTGTAA AACAAGGTGA TTCACATACA CAGACCAGTA ATGCTGTTCC TAAAGGGGCC 900
CAAGCTGATC CCATCAGTCA GCAGGGCTGC TCACAGGGCA CCTGGCCTGT CTTTGTTGAA 960
GGCGATTCCT GTGAAGGCAG TGGAGGAGCT CCGGGTGGGA GGTGAGTGTT GTGGAGAGCC 1020
CAGCAGCCCG CTGGGCTGAA CCTTGGACCA AGAACCAGTC TGTCCTTGGC TCCCTTGTGG 1080
GTGGGGAAAG ATGAGGTGTA TCAGGCAGGG TCCAGTCCAG AAACAGAAAC CAGAGCAACA 1140
ATCGTAGAGG CCGTTGTTCA GCCAGGTATT GAGAAAATAG AGAAGGCAAA AAGGGAACAC 1200
TGGTGTCGTG GAGGAGACCC CTGCCAGCAT TGGCTCCACA CAGCTGACCC TGGGATAAGA 1260
GAATTGTTGG ACTCTTTAGA ACCTGGAGCT GGGAAGGCAG GTGTCTGCCA GCTGGCGGGT 1320
GCTGGGAGTC TGTGGGGGCA TGCGATGAGG AATTCTGCTG GTGGAGGGAA AGCCACAAAG 1380
TGGATTCCGC TGCTGCTATG GGAAGGGACG GTCACTACCG CTGCCCCTGT GGGGAGAAGA 1440
GCCCCGGGGG AAGAAGAGCA CTGCTGACAG AAGCCCATTC TCTTCGCAGG CTTCAGTTTC 1500
ACATTCTTGG TACCTCCTGG TGGTGCCTGG GAGGGAGCCA CTGCTGTACA GAGATGCCAA 1560
TTCCAGAGGC ATGGTCCGGC ACAGAGCGCT GGCTTCCAGC TGAAGGACAT GTGTAACAGC 1620
AGGAGATACC TTTCTCTGGG GTCCCAGGCT CCCGTCCTGG ACCTTGGCAC CCCGCCCCCC 1680
GTGCATTGTC GTCTTCTGAG TCTGGCTTTG TCTGGCACAT GAAGTTGGAT GGGTAGACTC 1740
TGGAAGCGTC CAGACCAGCT TGCGATGCTG ATGAATAAGC TGATTTTGAT GGGGTGTGTG 1800
AAACGGAGAT GCCAGCCCAG GGGCTCAGCT TGCTCGTGCT CTCATTTAAA AGCAGAAAAT 1860
AGCGACTTCA TTCTCGGATA CGTTTGCCAG CCCCAAAGGA TTAATTATCT ACACACCCAG 1920
AAGCAGTGGA GCAGAATATT TTGGCAGGAT TTTCAGGATT TGTGTCATCG TTGCTTAATA 1980
TCTGTTTCTT CACAGTCGGT TAGAATTTTA AAGGATTTGA AATACTGCAA GCTATCTGTG 2040
TATAGAGGCT GTGGATTCGG GCTGGTACAT TTGCAAAGTG CCCATTTTAT TTTTTATTTT 2100
TATTTTTATG TTTTTTGAGA CATATTCTCA CTCCGTCACC CAGGCTAGAG TGCAGTGGTG 2160
CCATCAGGGC TCACTGCAGC CTCCACCTCC TGGGCTCAGT GATCCTCCCA CCTCAGCCTC 2220
CCGAGTAGCT GGGACTACAG ACATGTGCCA CCACGCCCGG CTAATTTCTG TATTTTTTGT 2280
AGAGACAGGG TTTTTGCCAT GTTGCCCAGG CTGGTCTTGA ACTCCTGGCC TCAAACTGTA 2340
CTCCTACCTC GGCCTCCTAA AGTGCTGGGA TTACAGGCAT GAGCCACTGC ACCTGGCCGC 2400
AAAAAAAGTT AAAGTGCTAA CTTTAACTTT TTAGATTAGT AAGACTGCTA ACGTGTTTCA 2460
TTAGTTCAGT GATAATACCG GCTTCAAAGA AAAGCCTTGG CAAATACAAA TCGTAAGCAG 2520
ATAGCTCAAC TCATCATCAC AAAGCAAAGC CCACCCAGTG AAGAAACAAA TGTGGGAAGC 2580
CCCGGAAGCC CCTCCCCATC CCCACCCCCC CCCCCGCCCC CCCCGCCCTG GAAACAGCCG 2640
CTGTCCTGGT GTTGACAGCA GAGGTGGCAC TGCCTGGCTT TGAACTTGAA GGTGGGACTC 2700
AGGGGTGGTT GGCTGTTCAG ATGCAGCAGG GAGAGAGGGT TTGGGGCATT GCTGGTGCAC 2760
GGGAGAGGGT GGGGATGGCC CCCCAAACTA GCGGAGGCCG GGCTTGGCCC TGGGAGATAC 2820
AGGAAGGAGG CCCCCACTCC GTGGATTCCG TCCTTCCTCT CCATCTGTCT GGAACCCTCA 2880
CCCTCTCCCT CCCTCTCTGT CCTCACACAC CCACTCCCTG ACTCTCACTC AGGCTTTTGA 2940
GGCATGTGTG CTGCCCGCGG AGCCCTTGGC CTGACTTCTT CCAAGGGGTG GGGTAGACGC 3000
CCACATTTTC ACAGCAGAGA CAGCCTCCCA GCCTCTGTTC AGTGTGTGGA CAGATGGGTA 3060
TTGCCTTCGT TTTATTGTTT GTTAGTCTTA TTGAGTGCTT TCGCTGGGTG CGATTTCTGG 3120
AATGATGCGT GAAGTGCTTC CCCATGGAGG TCCTGTGGGC TGGGCGATGC CCTCCCGGGC 3180
TGGTTGCTCC CCAGAGAGGG AAGCCCAGCT CCAGACACAC AAGGCCCTGC CTGTGCACAT 3240
GTCATGTGTG ACTCGGGGAG AGCCTCCTGC TCTGATGCGT CAGCCCTCCA GCCTGCAGCT 3300
GGGGGCCCCG TGCCAGCCGG GACTCATTTA CTCCCCTCTT CTGAGTCAGC ACCTGCTGGG 3360
GTTCGTGGGA CCCCAGACCT GGCTCTCTTA CGCCTACCTG TTCCTTCTCT 3410