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

TagContent
EnhancerAtlas ID
HS040-05147 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr10:105435290-105439700 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12357919chr10105438112hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Arid3bMA0601.1chr10:105438634-105438645ATATTAATTAG+6.02
POU2F2MA0507.1chr10:105439342-105439355AAATGCAAATGAG-6.28
RELMA0101.1chr10:105438096-105438106GGAAATCCCC-6.02
ZNF263MA0528.1chr10:105437985-105438006ACCCCATCCCTCCCCTCCTCT-6.43
ZNF263MA0528.1chr10:105439292-105439313GGAGGAAGGGTGGGGGAGAGG+6.5
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_01123chr10:105435818-105436833Adrenal_Gland
SE_01123chr10:105436863-105438098Adrenal_Gland
SE_03245chr10:105437303-105439516Brain_Angular_Gyrus
SE_04097chr10:105437063-105439633Brain_Anterior_Caudate
SE_04829chr10:105435922-105440058Brain_Cingulate_Gyrus
SE_05806chr10:105435511-105440047Brain_Hippocampus_Middle
SE_06868chr10:105435726-105439761Brain_Hippocampus_Middle_150
SE_07764chr10:105437028-105439764Brain_Inferior_Temporal_Lobe
SE_24302chr10:105437518-105438104Colon_Crypt_2
SE_27093chr10:105435708-105439716Esophagus
SE_28404chr10:105435793-105438963Fetal_Intestine
SE_29224chr10:105434879-105439016Fetal_Intestine_Large
SE_29876chr10:105435145-105439225Fetal_Muscle
SE_32187chr10:105435891-105438694Gastric
SE_37600chr10:105434487-105440061HSMMtube
SE_41304chr10:105435827-105438937Left_Ventricle
SE_42617chr10:105435858-105438869Lung
SE_44236chr10:105435104-105439872NHDF-Ad
SE_44930chr10:105435720-105438923NHLF
SE_45960chr10:105434772-105439542Osteoblasts
SE_46694chr10:105435929-105438617Ovary
SE_46694chr10:105438827-105439391Ovary
SE_49112chr10:105435785-105436832Right_Atrium
SE_49112chr10:105436875-105439024Right_Atrium
SE_50307chr10:105435832-105439762Sigmoid_Colon
SE_52745chr10:105435887-105439737Small_Intestine
SE_65658chr10:105435601-105439922Pancreatic_islets
SE_69111chr10:105435695-105436624H9
SE_69111chr10:105437721-105438564H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10105435771105439697
Number: 1             
IDChromosomeStartEnd
GH10I103675chr10105434760105439726
Enhancer Sequence
TGGAAGGACT ATTTAGGGTC TCAGAACCAG AGAGGAGAAG AGACTTGCCT AAGATCACAC 60
AGCAAATAAG TCGTAGGGCT GGAGCTAGAA TAATTATACC AGTTTCCACT TACTTAACAT 120
TCATGCTAGG TGCTGTGCTA AACATTTATG AGCATTTTCT TGTTTAATCT TCACAACAGT 180
CTGTAATTTA CAGATGAGGA AAGTGAGGCA CAGAAAAGTT AAGGCTCTGG CCTTGTGCGG 240
TGGCTCACGC CTGTAACCTT AGCACTTTGG GAGGCTGAGG TGGGTGGATC ATCTGAGGTC 300
AGGAGTTCGA GACCAGCCTG TCCAACATGT TAAACCCCAT CTCTACTAAA TATAAAATTA 360
GCCAGGCATA GTGGTGCATG CCTGTAATCT CAGCTACTTG GGCGGCTGAG GCAGGAGAAT 420
TGCTTGAATC CGGGAGGCGG AGGTTGCAGT GAGCCGAGAT CGCGCCATTG CACTCCAGCC 480
TGGGCAACAA GAGCGAAACT CCGTCTCGGG GGAAAAAAAA AAGAAAAGTT AAGGTTCTTT 540
CCCAAGGCCC TACAGCAAGA AGTGATGGCA TCAGACTTAA GCCCAGGCAG GCTGGCCAGG 600
AATTGGGAAC AAAGGGTCCT CATGGGGGAT GTCATTTTCT GATCCTCCCT GGCCACTGGC 660
CAAGGCTTTC TTTATTTCTG CTGCTTTTCG TAAATGCAGC AAGAAAGGAC TTGCCTCATT 720
CCCTGGAATC CAGAACACGT GTGGGGGCAG CCCAACCCAG GGTAGGAATG CACTATTGAC 780
CCTCTGGCCC TGGGTTATGC AGTCAAGGAG CAGTTTCCCT GCTCAGGCGG GGGATGGGGT 840
GCAGTGGGGG CTGGGCCTGG AGACCCTCCA CAGCCCCTTA GGGACTAAGT CCAAGGGTGC 900
CTGCCTAGGC CAAGCCTGGG GCCAGAAGGG TCAGCCCAGC CTAAGTGGGT GTGGACGGAG 960
AAGCCAAGGA TGCCCTAGGA GCACTGAGGC TGCCTAGAAG GGGCTGCCCT GGCAGGGAGT 1020
AGCAGGTAGT TCTGTCACCT CCCTCCACCC TGCTGAGAAG ACCGGAAGCT TCCTGGTTAA 1080
AGATAGGTGC TGGGTTAGTG AGAGGTGCCG TGGGTGGACA GAGGGGTGCT GGCCAGGGAG 1140
GCTGGCAGGT TCAGAGCCTC TCTGATCCCA GCAGCTGCTG CCCAACCCAT GGCAGCCCCT 1200
TGGGTTGCGG CCTCCCCCTC AGTTCTCAGG TTCTCACCTC TCCCCACCCC AGGGCATTTG 1260
TGTGCAGAGA AGAGACAAAC TCAAGTTTGT TCTGAGTTCC AGGATCCCAG CCACCTCCCT 1320
CCCTGGGGTG GCCTGCCTTG GTGGTCCTCC CTCACTTACT GGGAGATCCT CCCTCCAATT 1380
CCCCCACCCT CCAGCTCCCC CAGAAGCCCG AGCCAAAGCC AGTATTTGCG TTCACACAGA 1440
GAAGGAGCAG CAGAGAGGCT GGGCAGTGGG ATGAAGTCAG CAGTCGCTGG TCTCCAGCCC 1500
CGAGTCTTGC AATCCGCCTC CTCCCTGGCT CAGTCTCCCT GAGAGCCGCG AGTGAGTGAT 1560
GGAGTCAATA GCAACGGACT CAGGACAGAC ATTCCCCTCC CCGGACAACA AAATGTGGAA 1620
TGTCTCCTTC TCTCCAGACT GGACTCTTGC TATCGGATTA TCAATGAATC AACCGCCAAC 1680
TATTTCGGGA GCATCAACGG CCCCTGGTTG AGACCATCTG ACTCTCCACC CTCTGTCTCA 1740
AAGCATCAGA CACACAACCA CAGACACCGT CCCCAGCATT CCTGTCTGCT TCAGGAGTCA 1800
TGTAGGTTTG GGGAGACAGG CTGGGTCCCG GAAGGTCTGA GGGAGGAGAC GGCAGGGCTG 1860
AGTCCTGGAG GCCTTGAAGG TATAACTGGA CCCATCTTTG GGGTAGGGCT CACGGAGCCT 1920
CAGGGACATC TGGCTGGACG CTGCCATCCA CTGGTGCAAG ACAGGGGTGG GGATGGGGGG 1980
TCAGGGGTAG GAGGAGAATT CATTCCTGGA CTGAGGTTGA GGACACCCAC TTTTCAAGGT 2040
TTTCTGTCTC CCTTATCATG CCCTGGGCAG GATCTTTGTT CACTGACTGT TCCCACTGGC 2100
TCCAAACGTC TGGTTAGGGC TATAGTCCTA GCAAGCGCAT AGCGCATAGT AGGTGCTTAT 2160
TAAAGATTTG TTATGAGTCT CTTCAATCAG ACCTTTAGTT CCTTCAAGGC CTTATCCCTG 2220
TCAGCACCCC ACAACACCTT GAATGCAGGA GGTGCCCAAT TAACCCTCAG TGGCTGATGG 2280
AAAGATGAAT ACTCACTGCT CTCAAGCCCA AGGGTGCATG GAAAACTGAG GCCCGGCTAC 2340
CCCACTGCCC CAGGACCCTC TTGATACCCA CGGCTCTGCC CTCTCTAGTC CAGGCTTGGC 2400
CTCCGGAACC ACATACAGGC ATACAGGCCT GGCTTGTGCT GGGCACAGTG GCTCCCGTGC 2460
AGGCCTCCGA GCCTGCAGAA CACCCTGAAG GGCGTTGGCT CCCAGCATCT GCTTTAATGC 2520
CCTTCAAAGA GATTTTTAGA AAAATTACCC CTAAGCAGTA CAGTCTCTGG CAGGATGGAC 2580
GCTACAGGAA ACAGGAGCCG GAGCAGGAAC GACCCGTTCA TGTGTAATGT CTGGGGGGAG 2640
CAGGGCTTGG TGCAGCCTCC CATGGTGTTT GCTGGGAGCC CCTGAGCCTT TCCTTACCCC 2700
ATCCCTCCCC TCCTCTGCGT GGGTCCAGAC CAATCCCCTG AGCGCTGAGA TGCCACGTAA 2760
ACAGAGCTGT GCATGCACGC AGTGCGCACG CACACACCAC TGCTTGGGAA ATCCCCACAT 2820
CTGGCTCTCA CGTGACCCAG CTATGCCCAG AAGGCTGCAG CTGAGAGGGC CTGGAAGATG 2880
AGAGGGTCGG GAGTGTGCGG CTCTCTGGGG AGCCCCGAGT TAACCCTTCA GCACCACAGC 2940
TCGGCGGCTC TGTCTAATGC TAAGCTTCCA GAGAGGGGAG AAGCCAGGAA GGAGGCCTGG 3000
TGCTCAGTGC TCAGCCCTGG CCCTGGTTGC CTTTCCCAGC GTGGGAAGGT TGGGACACTT 3060
CTCTGGGCCT CACTGGTCTT GACCTGGGAT GTGAAAGGGC TGCTCTTTCC CTGTCCTGTC 3120
AATCCTGGTC AATCATCAGC CTCTCGGGAG TTCTCACTGG AGGGAGATTC CTTCCCTGAT 3180
GGAGGATATT TCATGTGCAT CTCCTAGTGT CAGGAACCTG GCTGCAGGAC AGTGATCCTG 3240
GAATCACAAG GAGTCAAGAT TCATGGCCTC CTTTGTCTCC CAGGAAACGG CTGGGCTCTT 3300
CCTAACAATA AGGAAAAGGT GGGAGGTGGC TCCTGGGCCA ACACATATTA ATTAGAACAT 3360
TTTAAACTTC AATAATTTTA TTGAACAAGT AGCAATCTGC AATAGCTCCT CTGAAACAGA 3420
ACCACACAGT AGGTGCTCCA GGGCTATGAA AGAGATGCCC CACATGGAAG ACGTGGCACA 3480
TGGGGACAGT GGCTCCTACC ACTGAACAGA TGTCCTCTGC ACAGGTACTG TCCTCTTCAC 3540
CCAGCTGACC CATTTAGAAA GCTCAGTAAA TTAGGCTCAG CAGCCATGCA GGTCTGTGTG 3600
CCTTGCTCAG AGACCCCTAC ATGGCGTGGC CCCAGCCCCG TGCAGCACTT GTGACACTGT 3660
TTTAAAACTG CTGTTTCCTT GCCCACCTCC CCCATCTGGC CAGGAGTCCT CTGAGGACAA 3720
GGACCTCATT GTCTCCATCT TGGTATCACT GAGGTTCCAT CACAAGACCT GTCAGATGTG 3780
CAGTAGACAA ACCTAGAAGG CAGGCACAGC CAGAGCCAGA AAAGCCAGCT TTAGTCTGGA 3840
AGGAGCCACC TCATCCCAGA AGGAAGACCT AGTACCAGTG TCCATTCAGA AACTTGCTTC 3900
CTATCCACTA GCCTTCAAGG GTACCCTCCC TGCGCCCCAG GAGACAGCTG CCTAGTGTCC 3960
ACTGAGCCAT GGGCTTGGAG CAGAAGGAGC GAGCCAAGTC ATGGAGGAAG GGTGGGGGAG 4020
AGGGGAGTTC CCCTGACCAG AACCCTGTGG CCAAATGCAA ATGAGCAACT CAGAGCCAGC 4080
AGGCTCCAGG ACTGTGTATG GCAGGAGCTC ACAGGCCAGA AGAACTTGTC CCACCCTGAC 4140
AGATCTGAAA TGAGGGATGT TAAAATCTGC ATATTTGCAA GGTCCCCCTG GGGGGGCCAT 4200
TGCCAACATA CAAAGACAGT CTTAGTTTGG TCTGTTGTCA CCAGCCTGTC ATCACTGCTT 4260
AGCATAGCAA GGATCTGACC CTCCAGCTGG GAAGTTATGT ACCCAGACCT GATCCTCTTC 4320
CAACACTCAA AGAGCCTAAG GTGCTCCAGG GCTGAGCTGA GGACACCCTT ACTCACAGGG 4380
ATCCAGAAGC AGTGACAAGG GGGAGGATGG 4410