EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS051-03799 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr10:105436760-105439560 
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
ATGAAGTCAG CAGTCGCTGG TCTCCAGCCC CGAGTCTTGC AATCCGCCTC CTCCCTGGCT 60
CAGTCTCCCT GAGAGCCGCG AGTGAGTGAT GGAGTCAATA GCAACGGACT CAGGACAGAC 120
ATTCCCCTCC CCGGACAACA AAATGTGGAA TGTCTCCTTC TCTCCAGACT GGACTCTTGC 180
TATCGGATTA TCAATGAATC AACCGCCAAC TATTTCGGGA GCATCAACGG CCCCTGGTTG 240
AGACCATCTG ACTCTCCACC CTCTGTCTCA AAGCATCAGA CACACAACCA CAGACACCGT 300
CCCCAGCATT CCTGTCTGCT TCAGGAGTCA TGTAGGTTTG GGGAGACAGG CTGGGTCCCG 360
GAAGGTCTGA GGGAGGAGAC GGCAGGGCTG AGTCCTGGAG GCCTTGAAGG TATAACTGGA 420
CCCATCTTTG GGGTAGGGCT CACGGAGCCT CAGGGACATC TGGCTGGACG CTGCCATCCA 480
CTGGTGCAAG ACAGGGGTGG GGATGGGGGG TCAGGGGTAG GAGGAGAATT CATTCCTGGA 540
CTGAGGTTGA GGACACCCAC TTTTCAAGGT TTTCTGTCTC CCTTATCATG CCCTGGGCAG 600
GATCTTTGTT CACTGACTGT TCCCACTGGC TCCAAACGTC TGGTTAGGGC TATAGTCCTA 660
GCAAGCGCAT AGCGCATAGT AGGTGCTTAT TAAAGATTTG TTATGAGTCT CTTCAATCAG 720
ACCTTTAGTT CCTTCAAGGC CTTATCCCTG TCAGCACCCC ACAACACCTT GAATGCAGGA 780
GGTGCCCAAT TAACCCTCAG TGGCTGATGG AAAGATGAAT ACTCACTGCT CTCAAGCCCA 840
AGGGTGCATG GAAAACTGAG GCCCGGCTAC CCCACTGCCC CAGGACCCTC TTGATACCCA 900
CGGCTCTGCC CTCTCTAGTC CAGGCTTGGC CTCCGGAACC ACATACAGGC ATACAGGCCT 960
GGCTTGTGCT GGGCACAGTG GCTCCCGTGC AGGCCTCCGA GCCTGCAGAA CACCCTGAAG 1020
GGCGTTGGCT CCCAGCATCT GCTTTAATGC CCTTCAAAGA GATTTTTAGA AAAATTACCC 1080
CTAAGCAGTA CAGTCTCTGG CAGGATGGAC GCTACAGGAA ACAGGAGCCG GAGCAGGAAC 1140
GACCCGTTCA TGTGTAATGT CTGGGGGGAG CAGGGCTTGG TGCAGCCTCC CATGGTGTTT 1200
GCTGGGAGCC CCTGAGCCTT TCCTTACCCC ATCCCTCCCC TCCTCTGCGT GGGTCCAGAC 1260
CAATCCCCTG AGCGCTGAGA TGCCACGTAA ACAGAGCTGT GCATGCACGC AGTGCGCACG 1320
CACACACCAC TGCTTGGGAA ATCCCCACAT CTGGCTCTCA CGTGACCCAG CTATGCCCAG 1380
AAGGCTGCAG CTGAGAGGGC CTGGAAGATG AGAGGGTCGG GAGTGTGCGG CTCTCTGGGG 1440
AGCCCCGAGT TAACCCTTCA GCACCACAGC TCGGCGGCTC TGTCTAATGC TAAGCTTCCA 1500
GAGAGGGGAG AAGCCAGGAA GGAGGCCTGG TGCTCAGTGC TCAGCCCTGG CCCTGGTTGC 1560
CTTTCCCAGC GTGGGAAGGT TGGGACACTT CTCTGGGCCT CACTGGTCTT GACCTGGGAT 1620
GTGAAAGGGC TGCTCTTTCC CTGTCCTGTC AATCCTGGTC AATCATCAGC CTCTCGGGAG 1680
TTCTCACTGG AGGGAGATTC CTTCCCTGAT GGAGGATATT TCATGTGCAT CTCCTAGTGT 1740
CAGGAACCTG GCTGCAGGAC AGTGATCCTG GAATCACAAG GAGTCAAGAT TCATGGCCTC 1800
CTTTGTCTCC CAGGAAACGG CTGGGCTCTT CCTAACAATA AGGAAAAGGT GGGAGGTGGC 1860
TCCTGGGCCA ACACATATTA ATTAGAACAT TTTAAACTTC AATAATTTTA TTGAACAAGT 1920
AGCAATCTGC AATAGCTCCT CTGAAACAGA ACCACACAGT AGGTGCTCCA GGGCTATGAA 1980
AGAGATGCCC CACATGGAAG ACGTGGCACA TGGGGACAGT GGCTCCTACC ACTGAACAGA 2040
TGTCCTCTGC ACAGGTACTG TCCTCTTCAC CCAGCTGACC CATTTAGAAA GCTCAGTAAA 2100
TTAGGCTCAG CAGCCATGCA GGTCTGTGTG CCTTGCTCAG AGACCCCTAC ATGGCGTGGC 2160
CCCAGCCCCG TGCAGCACTT GTGACACTGT TTTAAAACTG CTGTTTCCTT GCCCACCTCC 2220
CCCATCTGGC CAGGAGTCCT CTGAGGACAA GGACCTCATT GTCTCCATCT TGGTATCACT 2280
GAGGTTCCAT CACAAGACCT GTCAGATGTG CAGTAGACAA ACCTAGAAGG CAGGCACAGC 2340
CAGAGCCAGA AAAGCCAGCT TTAGTCTGGA AGGAGCCACC TCATCCCAGA AGGAAGACCT 2400
AGTACCAGTG TCCATTCAGA AACTTGCTTC CTATCCACTA GCCTTCAAGG GTACCCTCCC 2460
TGCGCCCCAG GAGACAGCTG CCTAGTGTCC ACTGAGCCAT GGGCTTGGAG CAGAAGGAGC 2520
GAGCCAAGTC ATGGAGGAAG GGTGGGGGAG AGGGGAGTTC CCCTGACCAG AACCCTGTGG 2580
CCAAATGCAA ATGAGCAACT CAGAGCCAGC AGGCTCCAGG ACTGTGTATG GCAGGAGCTC 2640
ACAGGCCAGA AGAACTTGTC CCACCCTGAC AGATCTGAAA TGAGGGATGT TAAAATCTGC 2700
ATATTTGCAA GGTCCCCCTG GGGGGGCCAT TGCCAACATA CAAAGACAGT CTTAGTTTGG 2760
TCTGTTGTCA CCAGCCTGTC ATCACTGCTT AGCATAGCAA 2800