EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS061-03331 
Organism
Homo sapiens 
Tissue/cell
GM12892 
Coordinate
chr10:105436840-105439720 
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
AGTGAGTGAT GGAGTCAATA GCAACGGACT CAGGACAGAC ATTCCCCTCC CCGGACAACA 60
AAATGTGGAA TGTCTCCTTC TCTCCAGACT GGACTCTTGC TATCGGATTA TCAATGAATC 120
AACCGCCAAC TATTTCGGGA GCATCAACGG CCCCTGGTTG AGACCATCTG ACTCTCCACC 180
CTCTGTCTCA AAGCATCAGA CACACAACCA CAGACACCGT CCCCAGCATT CCTGTCTGCT 240
TCAGGAGTCA TGTAGGTTTG GGGAGACAGG CTGGGTCCCG GAAGGTCTGA GGGAGGAGAC 300
GGCAGGGCTG AGTCCTGGAG GCCTTGAAGG TATAACTGGA CCCATCTTTG GGGTAGGGCT 360
CACGGAGCCT CAGGGACATC TGGCTGGACG CTGCCATCCA CTGGTGCAAG ACAGGGGTGG 420
GGATGGGGGG TCAGGGGTAG GAGGAGAATT CATTCCTGGA CTGAGGTTGA GGACACCCAC 480
TTTTCAAGGT TTTCTGTCTC CCTTATCATG CCCTGGGCAG GATCTTTGTT CACTGACTGT 540
TCCCACTGGC TCCAAACGTC TGGTTAGGGC TATAGTCCTA GCAAGCGCAT AGCGCATAGT 600
AGGTGCTTAT TAAAGATTTG TTATGAGTCT CTTCAATCAG ACCTTTAGTT CCTTCAAGGC 660
CTTATCCCTG TCAGCACCCC ACAACACCTT GAATGCAGGA GGTGCCCAAT TAACCCTCAG 720
TGGCTGATGG AAAGATGAAT ACTCACTGCT CTCAAGCCCA AGGGTGCATG GAAAACTGAG 780
GCCCGGCTAC CCCACTGCCC CAGGACCCTC TTGATACCCA CGGCTCTGCC CTCTCTAGTC 840
CAGGCTTGGC CTCCGGAACC ACATACAGGC ATACAGGCCT GGCTTGTGCT GGGCACAGTG 900
GCTCCCGTGC AGGCCTCCGA GCCTGCAGAA CACCCTGAAG GGCGTTGGCT CCCAGCATCT 960
GCTTTAATGC CCTTCAAAGA GATTTTTAGA AAAATTACCC CTAAGCAGTA CAGTCTCTGG 1020
CAGGATGGAC GCTACAGGAA ACAGGAGCCG GAGCAGGAAC GACCCGTTCA TGTGTAATGT 1080
CTGGGGGGAG CAGGGCTTGG TGCAGCCTCC CATGGTGTTT GCTGGGAGCC CCTGAGCCTT 1140
TCCTTACCCC ATCCCTCCCC TCCTCTGCGT GGGTCCAGAC CAATCCCCTG AGCGCTGAGA 1200
TGCCACGTAA ACAGAGCTGT GCATGCACGC AGTGCGCACG CACACACCAC TGCTTGGGAA 1260
ATCCCCACAT CTGGCTCTCA CGTGACCCAG CTATGCCCAG AAGGCTGCAG CTGAGAGGGC 1320
CTGGAAGATG AGAGGGTCGG GAGTGTGCGG CTCTCTGGGG AGCCCCGAGT TAACCCTTCA 1380
GCACCACAGC TCGGCGGCTC TGTCTAATGC TAAGCTTCCA GAGAGGGGAG AAGCCAGGAA 1440
GGAGGCCTGG TGCTCAGTGC TCAGCCCTGG CCCTGGTTGC CTTTCCCAGC GTGGGAAGGT 1500
TGGGACACTT CTCTGGGCCT CACTGGTCTT GACCTGGGAT GTGAAAGGGC TGCTCTTTCC 1560
CTGTCCTGTC AATCCTGGTC AATCATCAGC CTCTCGGGAG TTCTCACTGG AGGGAGATTC 1620
CTTCCCTGAT GGAGGATATT TCATGTGCAT CTCCTAGTGT CAGGAACCTG GCTGCAGGAC 1680
AGTGATCCTG GAATCACAAG GAGTCAAGAT TCATGGCCTC CTTTGTCTCC CAGGAAACGG 1740
CTGGGCTCTT CCTAACAATA AGGAAAAGGT GGGAGGTGGC TCCTGGGCCA ACACATATTA 1800
ATTAGAACAT TTTAAACTTC AATAATTTTA TTGAACAAGT AGCAATCTGC AATAGCTCCT 1860
CTGAAACAGA ACCACACAGT AGGTGCTCCA GGGCTATGAA AGAGATGCCC CACATGGAAG 1920
ACGTGGCACA TGGGGACAGT GGCTCCTACC ACTGAACAGA TGTCCTCTGC ACAGGTACTG 1980
TCCTCTTCAC CCAGCTGACC CATTTAGAAA GCTCAGTAAA TTAGGCTCAG CAGCCATGCA 2040
GGTCTGTGTG CCTTGCTCAG AGACCCCTAC ATGGCGTGGC CCCAGCCCCG TGCAGCACTT 2100
GTGACACTGT TTTAAAACTG CTGTTTCCTT GCCCACCTCC CCCATCTGGC CAGGAGTCCT 2160
CTGAGGACAA GGACCTCATT GTCTCCATCT TGGTATCACT GAGGTTCCAT CACAAGACCT 2220
GTCAGATGTG CAGTAGACAA ACCTAGAAGG CAGGCACAGC CAGAGCCAGA AAAGCCAGCT 2280
TTAGTCTGGA AGGAGCCACC TCATCCCAGA AGGAAGACCT AGTACCAGTG TCCATTCAGA 2340
AACTTGCTTC CTATCCACTA GCCTTCAAGG GTACCCTCCC TGCGCCCCAG GAGACAGCTG 2400
CCTAGTGTCC ACTGAGCCAT GGGCTTGGAG CAGAAGGAGC GAGCCAAGTC ATGGAGGAAG 2460
GGTGGGGGAG AGGGGAGTTC CCCTGACCAG AACCCTGTGG CCAAATGCAA ATGAGCAACT 2520
CAGAGCCAGC AGGCTCCAGG ACTGTGTATG GCAGGAGCTC ACAGGCCAGA AGAACTTGTC 2580
CCACCCTGAC AGATCTGAAA TGAGGGATGT TAAAATCTGC ATATTTGCAA GGTCCCCCTG 2640
GGGGGGCCAT TGCCAACATA CAAAGACAGT CTTAGTTTGG TCTGTTGTCA CCAGCCTGTC 2700
ATCACTGCTT AGCATAGCAA GGATCTGACC CTCCAGCTGG GAAGTTATGT ACCCAGACCT 2760
GATCCTCTTC CAACACTCAA AGAGCCTAAG GTGCTCCAGG GCTGAGCTGA GGACACCCTT 2820
ACTCACAGGG ATCCAGAAGC AGTGACAAGG GGGAGGATGG TGAAGAGATG GCCAGCTCTG 2880