EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-04784 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr10:105436870-105439840 
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
CAGGACAGAC ATTCCCCTCC CCGGACAACA AAATGTGGAA TGTCTCCTTC TCTCCAGACT 60
GGACTCTTGC TATCGGATTA TCAATGAATC AACCGCCAAC TATTTCGGGA GCATCAACGG 120
CCCCTGGTTG AGACCATCTG ACTCTCCACC CTCTGTCTCA AAGCATCAGA CACACAACCA 180
CAGACACCGT CCCCAGCATT CCTGTCTGCT TCAGGAGTCA TGTAGGTTTG GGGAGACAGG 240
CTGGGTCCCG GAAGGTCTGA GGGAGGAGAC GGCAGGGCTG AGTCCTGGAG GCCTTGAAGG 300
TATAACTGGA CCCATCTTTG GGGTAGGGCT CACGGAGCCT CAGGGACATC TGGCTGGACG 360
CTGCCATCCA CTGGTGCAAG ACAGGGGTGG GGATGGGGGG TCAGGGGTAG GAGGAGAATT 420
CATTCCTGGA CTGAGGTTGA GGACACCCAC TTTTCAAGGT TTTCTGTCTC CCTTATCATG 480
CCCTGGGCAG GATCTTTGTT CACTGACTGT TCCCACTGGC TCCAAACGTC TGGTTAGGGC 540
TATAGTCCTA GCAAGCGCAT AGCGCATAGT AGGTGCTTAT TAAAGATTTG TTATGAGTCT 600
CTTCAATCAG ACCTTTAGTT CCTTCAAGGC CTTATCCCTG TCAGCACCCC ACAACACCTT 660
GAATGCAGGA GGTGCCCAAT TAACCCTCAG TGGCTGATGG AAAGATGAAT ACTCACTGCT 720
CTCAAGCCCA AGGGTGCATG GAAAACTGAG GCCCGGCTAC CCCACTGCCC CAGGACCCTC 780
TTGATACCCA CGGCTCTGCC CTCTCTAGTC CAGGCTTGGC CTCCGGAACC ACATACAGGC 840
ATACAGGCCT GGCTTGTGCT GGGCACAGTG GCTCCCGTGC AGGCCTCCGA GCCTGCAGAA 900
CACCCTGAAG GGCGTTGGCT CCCAGCATCT GCTTTAATGC CCTTCAAAGA GATTTTTAGA 960
AAAATTACCC CTAAGCAGTA CAGTCTCTGG CAGGATGGAC GCTACAGGAA ACAGGAGCCG 1020
GAGCAGGAAC GACCCGTTCA TGTGTAATGT CTGGGGGGAG CAGGGCTTGG TGCAGCCTCC 1080
CATGGTGTTT GCTGGGAGCC CCTGAGCCTT TCCTTACCCC ATCCCTCCCC TCCTCTGCGT 1140
GGGTCCAGAC CAATCCCCTG AGCGCTGAGA TGCCACGTAA ACAGAGCTGT GCATGCACGC 1200
AGTGCGCACG CACACACCAC TGCTTGGGAA ATCCCCACAT CTGGCTCTCA CGTGACCCAG 1260
CTATGCCCAG AAGGCTGCAG CTGAGAGGGC CTGGAAGATG AGAGGGTCGG GAGTGTGCGG 1320
CTCTCTGGGG AGCCCCGAGT TAACCCTTCA GCACCACAGC TCGGCGGCTC TGTCTAATGC 1380
TAAGCTTCCA GAGAGGGGAG AAGCCAGGAA GGAGGCCTGG TGCTCAGTGC TCAGCCCTGG 1440
CCCTGGTTGC CTTTCCCAGC GTGGGAAGGT TGGGACACTT CTCTGGGCCT CACTGGTCTT 1500
GACCTGGGAT GTGAAAGGGC TGCTCTTTCC CTGTCCTGTC AATCCTGGTC AATCATCAGC 1560
CTCTCGGGAG TTCTCACTGG AGGGAGATTC CTTCCCTGAT GGAGGATATT TCATGTGCAT 1620
CTCCTAGTGT CAGGAACCTG GCTGCAGGAC AGTGATCCTG GAATCACAAG GAGTCAAGAT 1680
TCATGGCCTC CTTTGTCTCC CAGGAAACGG CTGGGCTCTT CCTAACAATA AGGAAAAGGT 1740
GGGAGGTGGC TCCTGGGCCA ACACATATTA ATTAGAACAT TTTAAACTTC AATAATTTTA 1800
TTGAACAAGT AGCAATCTGC AATAGCTCCT CTGAAACAGA ACCACACAGT AGGTGCTCCA 1860
GGGCTATGAA AGAGATGCCC CACATGGAAG ACGTGGCACA TGGGGACAGT GGCTCCTACC 1920
ACTGAACAGA TGTCCTCTGC ACAGGTACTG TCCTCTTCAC CCAGCTGACC CATTTAGAAA 1980
GCTCAGTAAA TTAGGCTCAG CAGCCATGCA GGTCTGTGTG CCTTGCTCAG AGACCCCTAC 2040
ATGGCGTGGC CCCAGCCCCG TGCAGCACTT GTGACACTGT TTTAAAACTG CTGTTTCCTT 2100
GCCCACCTCC CCCATCTGGC CAGGAGTCCT CTGAGGACAA GGACCTCATT GTCTCCATCT 2160
TGGTATCACT GAGGTTCCAT CACAAGACCT GTCAGATGTG CAGTAGACAA ACCTAGAAGG 2220
CAGGCACAGC CAGAGCCAGA AAAGCCAGCT TTAGTCTGGA AGGAGCCACC TCATCCCAGA 2280
AGGAAGACCT AGTACCAGTG TCCATTCAGA AACTTGCTTC CTATCCACTA GCCTTCAAGG 2340
GTACCCTCCC TGCGCCCCAG GAGACAGCTG CCTAGTGTCC ACTGAGCCAT GGGCTTGGAG 2400
CAGAAGGAGC GAGCCAAGTC ATGGAGGAAG GGTGGGGGAG AGGGGAGTTC CCCTGACCAG 2460
AACCCTGTGG CCAAATGCAA ATGAGCAACT CAGAGCCAGC AGGCTCCAGG ACTGTGTATG 2520
GCAGGAGCTC ACAGGCCAGA AGAACTTGTC CCACCCTGAC AGATCTGAAA TGAGGGATGT 2580
TAAAATCTGC ATATTTGCAA GGTCCCCCTG GGGGGGCCAT TGCCAACATA CAAAGACAGT 2640
CTTAGTTTGG TCTGTTGTCA CCAGCCTGTC ATCACTGCTT AGCATAGCAA GGATCTGACC 2700
CTCCAGCTGG GAAGTTATGT ACCCAGACCT GATCCTCTTC CAACACTCAA AGAGCCTAAG 2760
GTGCTCCAGG GCTGAGCTGA GGACACCCTT ACTCACAGGG ATCCAGAAGC AGTGACAAGG 2820
GGGAGGATGG TGAAGAGATG GCCAGCTCTG CCTTCTCTTT TATTTTATTT ATTTATTTAT 2880
TTTTTGAGAT AGAGTCTCGC TCTGTCACCC AGGCTGGAGT GCAATGGCGC CATCTCTGCT 2940
CACTGCAACC TCTGCCTCCC CGGTTCAAGT 2970