EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS127-04618 
Organism
Homo sapiens 
Tissue/cell
Macrophage 
Coordinate
chr10:105437500-105439900 
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
CTTATCCCTG TCAGCACCCC ACAACACCTT GAATGCAGGA GGTGCCCAAT TAACCCTCAG 60
TGGCTGATGG AAAGATGAAT ACTCACTGCT CTCAAGCCCA AGGGTGCATG GAAAACTGAG 120
GCCCGGCTAC CCCACTGCCC CAGGACCCTC TTGATACCCA CGGCTCTGCC CTCTCTAGTC 180
CAGGCTTGGC CTCCGGAACC ACATACAGGC ATACAGGCCT GGCTTGTGCT GGGCACAGTG 240
GCTCCCGTGC AGGCCTCCGA GCCTGCAGAA CACCCTGAAG GGCGTTGGCT CCCAGCATCT 300
GCTTTAATGC CCTTCAAAGA GATTTTTAGA AAAATTACCC CTAAGCAGTA CAGTCTCTGG 360
CAGGATGGAC GCTACAGGAA ACAGGAGCCG GAGCAGGAAC GACCCGTTCA TGTGTAATGT 420
CTGGGGGGAG CAGGGCTTGG TGCAGCCTCC CATGGTGTTT GCTGGGAGCC CCTGAGCCTT 480
TCCTTACCCC ATCCCTCCCC TCCTCTGCGT GGGTCCAGAC CAATCCCCTG AGCGCTGAGA 540
TGCCACGTAA ACAGAGCTGT GCATGCACGC AGTGCGCACG CACACACCAC TGCTTGGGAA 600
ATCCCCACAT CTGGCTCTCA CGTGACCCAG CTATGCCCAG AAGGCTGCAG CTGAGAGGGC 660
CTGGAAGATG AGAGGGTCGG GAGTGTGCGG CTCTCTGGGG AGCCCCGAGT TAACCCTTCA 720
GCACCACAGC TCGGCGGCTC TGTCTAATGC TAAGCTTCCA GAGAGGGGAG AAGCCAGGAA 780
GGAGGCCTGG TGCTCAGTGC TCAGCCCTGG CCCTGGTTGC CTTTCCCAGC GTGGGAAGGT 840
TGGGACACTT CTCTGGGCCT CACTGGTCTT GACCTGGGAT GTGAAAGGGC TGCTCTTTCC 900
CTGTCCTGTC AATCCTGGTC AATCATCAGC CTCTCGGGAG TTCTCACTGG AGGGAGATTC 960
CTTCCCTGAT GGAGGATATT TCATGTGCAT CTCCTAGTGT CAGGAACCTG GCTGCAGGAC 1020
AGTGATCCTG GAATCACAAG GAGTCAAGAT TCATGGCCTC CTTTGTCTCC CAGGAAACGG 1080
CTGGGCTCTT CCTAACAATA AGGAAAAGGT GGGAGGTGGC TCCTGGGCCA ACACATATTA 1140
ATTAGAACAT TTTAAACTTC AATAATTTTA TTGAACAAGT AGCAATCTGC AATAGCTCCT 1200
CTGAAACAGA ACCACACAGT AGGTGCTCCA GGGCTATGAA AGAGATGCCC CACATGGAAG 1260
ACGTGGCACA TGGGGACAGT GGCTCCTACC ACTGAACAGA TGTCCTCTGC ACAGGTACTG 1320
TCCTCTTCAC CCAGCTGACC CATTTAGAAA GCTCAGTAAA TTAGGCTCAG CAGCCATGCA 1380
GGTCTGTGTG CCTTGCTCAG AGACCCCTAC ATGGCGTGGC CCCAGCCCCG TGCAGCACTT 1440
GTGACACTGT TTTAAAACTG CTGTTTCCTT GCCCACCTCC CCCATCTGGC CAGGAGTCCT 1500
CTGAGGACAA GGACCTCATT GTCTCCATCT TGGTATCACT GAGGTTCCAT CACAAGACCT 1560
GTCAGATGTG CAGTAGACAA ACCTAGAAGG CAGGCACAGC CAGAGCCAGA AAAGCCAGCT 1620
TTAGTCTGGA AGGAGCCACC TCATCCCAGA AGGAAGACCT AGTACCAGTG TCCATTCAGA 1680
AACTTGCTTC CTATCCACTA GCCTTCAAGG GTACCCTCCC TGCGCCCCAG GAGACAGCTG 1740
CCTAGTGTCC ACTGAGCCAT GGGCTTGGAG CAGAAGGAGC GAGCCAAGTC ATGGAGGAAG 1800
GGTGGGGGAG AGGGGAGTTC CCCTGACCAG AACCCTGTGG CCAAATGCAA ATGAGCAACT 1860
CAGAGCCAGC AGGCTCCAGG ACTGTGTATG GCAGGAGCTC ACAGGCCAGA AGAACTTGTC 1920
CCACCCTGAC AGATCTGAAA TGAGGGATGT TAAAATCTGC ATATTTGCAA GGTCCCCCTG 1980
GGGGGGCCAT TGCCAACATA CAAAGACAGT CTTAGTTTGG TCTGTTGTCA CCAGCCTGTC 2040
ATCACTGCTT AGCATAGCAA GGATCTGACC CTCCAGCTGG GAAGTTATGT ACCCAGACCT 2100
GATCCTCTTC CAACACTCAA AGAGCCTAAG GTGCTCCAGG GCTGAGCTGA GGACACCCTT 2160
ACTCACAGGG ATCCAGAAGC AGTGACAAGG GGGAGGATGG TGAAGAGATG GCCAGCTCTG 2220
CCTTCTCTTT TATTTTATTT ATTTATTTAT TTTTTGAGAT AGAGTCTCGC TCTGTCACCC 2280
AGGCTGGAGT GCAATGGCGC CATCTCTGCT CACTGCAACC TCTGCCTCCC CGGTTCAAGT 2340
GATTCTCCTG CCTCAGCCTC CTGAGTAACT GGGATTACAG GCGCCCACCA CGACACCAAG 2400