EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-01994 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr10:105437440-105439710 
Target genes
Number: 5             
NameEnsembl ID
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: 28             
IDCoordinateTissue/cell
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_24302chr10:105438157-105438547Colon_Crypt_2
SE_24302chr10:105438683-105439050Colon_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_49112chr10:105436875-105439024Right_Atrium
SE_50307chr10:105435832-105439762Sigmoid_Colon
SE_52745chr10:105435887-105439737Small_Intestine
SE_65658chr10:105435601-105439922Pancreatic_islets
SE_69111chr10:105437721-105438564H9
Number: 1             
IDChromosomeStartEnd
GH10I103675chr10105434760105439726
Enhancer Sequence
AGGTGCTTAT TAAAGATTTG TTATGAGTCT CTTCAATCAG ACCTTTAGTT CCTTCAAGGC 60
CTTATCCCTG TCAGCACCCC ACAACACCTT GAATGCAGGA GGTGCCCAAT TAACCCTCAG 120
TGGCTGATGG AAAGATGAAT ACTCACTGCT CTCAAGCCCA AGGGTGCATG GAAAACTGAG 180
GCCCGGCTAC CCCACTGCCC CAGGACCCTC TTGATACCCA CGGCTCTGCC CTCTCTAGTC 240
CAGGCTTGGC CTCCGGAACC ACATACAGGC ATACAGGCCT GGCTTGTGCT GGGCACAGTG 300
GCTCCCGTGC AGGCCTCCGA GCCTGCAGAA CACCCTGAAG GGCGTTGGCT CCCAGCATCT 360
GCTTTAATGC CCTTCAAAGA GATTTTTAGA AAAATTACCC CTAAGCAGTA CAGTCTCTGG 420
CAGGATGGAC GCTACAGGAA ACAGGAGCCG GAGCAGGAAC GACCCGTTCA TGTGTAATGT 480
CTGGGGGGAG CAGGGCTTGG TGCAGCCTCC CATGGTGTTT GCTGGGAGCC CCTGAGCCTT 540
TCCTTACCCC ATCCCTCCCC TCCTCTGCGT GGGTCCAGAC CAATCCCCTG AGCGCTGAGA 600
TGCCACGTAA ACAGAGCTGT GCATGCACGC AGTGCGCACG CACACACCAC TGCTTGGGAA 660
ATCCCCACAT CTGGCTCTCA CGTGACCCAG CTATGCCCAG AAGGCTGCAG CTGAGAGGGC 720
CTGGAAGATG AGAGGGTCGG GAGTGTGCGG CTCTCTGGGG AGCCCCGAGT TAACCCTTCA 780
GCACCACAGC TCGGCGGCTC TGTCTAATGC TAAGCTTCCA GAGAGGGGAG AAGCCAGGAA 840
GGAGGCCTGG TGCTCAGTGC TCAGCCCTGG CCCTGGTTGC CTTTCCCAGC GTGGGAAGGT 900
TGGGACACTT CTCTGGGCCT CACTGGTCTT GACCTGGGAT GTGAAAGGGC TGCTCTTTCC 960
CTGTCCTGTC AATCCTGGTC AATCATCAGC CTCTCGGGAG TTCTCACTGG AGGGAGATTC 1020
CTTCCCTGAT GGAGGATATT TCATGTGCAT CTCCTAGTGT CAGGAACCTG GCTGCAGGAC 1080
AGTGATCCTG GAATCACAAG GAGTCAAGAT TCATGGCCTC CTTTGTCTCC CAGGAAACGG 1140
CTGGGCTCTT CCTAACAATA AGGAAAAGGT GGGAGGTGGC TCCTGGGCCA ACACATATTA 1200
ATTAGAACAT TTTAAACTTC AATAATTTTA TTGAACAAGT AGCAATCTGC AATAGCTCCT 1260
CTGAAACAGA ACCACACAGT AGGTGCTCCA GGGCTATGAA AGAGATGCCC CACATGGAAG 1320
ACGTGGCACA TGGGGACAGT GGCTCCTACC ACTGAACAGA TGTCCTCTGC ACAGGTACTG 1380
TCCTCTTCAC CCAGCTGACC CATTTAGAAA GCTCAGTAAA TTAGGCTCAG CAGCCATGCA 1440
GGTCTGTGTG CCTTGCTCAG AGACCCCTAC ATGGCGTGGC CCCAGCCCCG TGCAGCACTT 1500
GTGACACTGT TTTAAAACTG CTGTTTCCTT GCCCACCTCC CCCATCTGGC CAGGAGTCCT 1560
CTGAGGACAA GGACCTCATT GTCTCCATCT TGGTATCACT GAGGTTCCAT CACAAGACCT 1620
GTCAGATGTG CAGTAGACAA ACCTAGAAGG CAGGCACAGC CAGAGCCAGA AAAGCCAGCT 1680
TTAGTCTGGA AGGAGCCACC TCATCCCAGA AGGAAGACCT AGTACCAGTG TCCATTCAGA 1740
AACTTGCTTC CTATCCACTA GCCTTCAAGG GTACCCTCCC TGCGCCCCAG GAGACAGCTG 1800
CCTAGTGTCC ACTGAGCCAT GGGCTTGGAG CAGAAGGAGC GAGCCAAGTC ATGGAGGAAG 1860
GGTGGGGGAG AGGGGAGTTC CCCTGACCAG AACCCTGTGG CCAAATGCAA ATGAGCAACT 1920
CAGAGCCAGC AGGCTCCAGG ACTGTGTATG GCAGGAGCTC ACAGGCCAGA AGAACTTGTC 1980
CCACCCTGAC AGATCTGAAA TGAGGGATGT TAAAATCTGC ATATTTGCAA GGTCCCCCTG 2040
GGGGGGCCAT TGCCAACATA CAAAGACAGT CTTAGTTTGG TCTGTTGTCA CCAGCCTGTC 2100
ATCACTGCTT AGCATAGCAA GGATCTGACC CTCCAGCTGG GAAGTTATGT ACCCAGACCT 2160
GATCCTCTTC CAACACTCAA AGAGCCTAAG GTGCTCCAGG GCTGAGCTGA GGACACCCTT 2220
ACTCACAGGG ATCCAGAAGC AGTGACAAGG GGGAGGATGG TGAAGAGATG 2270