EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS188-01877 
Organism
Homo sapiens 
Tissue/cell
Th2 
Coordinate
chr10:105436810-105439480 
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
CTCCCTGGCT CAGTCTCCCT GAGAGCCGCG AGTGAGTGAT GGAGTCAATA GCAACGGACT 60
CAGGACAGAC ATTCCCCTCC CCGGACAACA AAATGTGGAA TGTCTCCTTC TCTCCAGACT 120
GGACTCTTGC TATCGGATTA TCAATGAATC AACCGCCAAC TATTTCGGGA GCATCAACGG 180
CCCCTGGTTG AGACCATCTG ACTCTCCACC CTCTGTCTCA AAGCATCAGA CACACAACCA 240
CAGACACCGT CCCCAGCATT CCTGTCTGCT TCAGGAGTCA TGTAGGTTTG GGGAGACAGG 300
CTGGGTCCCG GAAGGTCTGA GGGAGGAGAC GGCAGGGCTG AGTCCTGGAG GCCTTGAAGG 360
TATAACTGGA CCCATCTTTG GGGTAGGGCT CACGGAGCCT CAGGGACATC TGGCTGGACG 420
CTGCCATCCA CTGGTGCAAG ACAGGGGTGG GGATGGGGGG TCAGGGGTAG GAGGAGAATT 480
CATTCCTGGA CTGAGGTTGA GGACACCCAC TTTTCAAGGT TTTCTGTCTC CCTTATCATG 540
CCCTGGGCAG GATCTTTGTT CACTGACTGT TCCCACTGGC TCCAAACGTC TGGTTAGGGC 600
TATAGTCCTA GCAAGCGCAT AGCGCATAGT AGGTGCTTAT TAAAGATTTG TTATGAGTCT 660
CTTCAATCAG ACCTTTAGTT CCTTCAAGGC CTTATCCCTG TCAGCACCCC ACAACACCTT 720
GAATGCAGGA GGTGCCCAAT TAACCCTCAG TGGCTGATGG AAAGATGAAT ACTCACTGCT 780
CTCAAGCCCA AGGGTGCATG GAAAACTGAG GCCCGGCTAC CCCACTGCCC CAGGACCCTC 840
TTGATACCCA CGGCTCTGCC CTCTCTAGTC CAGGCTTGGC CTCCGGAACC ACATACAGGC 900
ATACAGGCCT GGCTTGTGCT GGGCACAGTG GCTCCCGTGC AGGCCTCCGA GCCTGCAGAA 960
CACCCTGAAG GGCGTTGGCT CCCAGCATCT GCTTTAATGC CCTTCAAAGA GATTTTTAGA 1020
AAAATTACCC CTAAGCAGTA CAGTCTCTGG CAGGATGGAC GCTACAGGAA ACAGGAGCCG 1080
GAGCAGGAAC GACCCGTTCA TGTGTAATGT CTGGGGGGAG CAGGGCTTGG TGCAGCCTCC 1140
CATGGTGTTT GCTGGGAGCC CCTGAGCCTT TCCTTACCCC ATCCCTCCCC TCCTCTGCGT 1200
GGGTCCAGAC CAATCCCCTG AGCGCTGAGA TGCCACGTAA ACAGAGCTGT GCATGCACGC 1260
AGTGCGCACG CACACACCAC TGCTTGGGAA ATCCCCACAT CTGGCTCTCA CGTGACCCAG 1320
CTATGCCCAG AAGGCTGCAG CTGAGAGGGC CTGGAAGATG AGAGGGTCGG GAGTGTGCGG 1380
CTCTCTGGGG AGCCCCGAGT TAACCCTTCA GCACCACAGC TCGGCGGCTC TGTCTAATGC 1440
TAAGCTTCCA GAGAGGGGAG AAGCCAGGAA GGAGGCCTGG TGCTCAGTGC TCAGCCCTGG 1500
CCCTGGTTGC CTTTCCCAGC GTGGGAAGGT TGGGACACTT CTCTGGGCCT CACTGGTCTT 1560
GACCTGGGAT GTGAAAGGGC TGCTCTTTCC CTGTCCTGTC AATCCTGGTC AATCATCAGC 1620
CTCTCGGGAG TTCTCACTGG AGGGAGATTC CTTCCCTGAT GGAGGATATT TCATGTGCAT 1680
CTCCTAGTGT CAGGAACCTG GCTGCAGGAC AGTGATCCTG GAATCACAAG GAGTCAAGAT 1740
TCATGGCCTC CTTTGTCTCC CAGGAAACGG CTGGGCTCTT CCTAACAATA AGGAAAAGGT 1800
GGGAGGTGGC TCCTGGGCCA ACACATATTA ATTAGAACAT TTTAAACTTC AATAATTTTA 1860
TTGAACAAGT AGCAATCTGC AATAGCTCCT CTGAAACAGA ACCACACAGT AGGTGCTCCA 1920
GGGCTATGAA AGAGATGCCC CACATGGAAG ACGTGGCACA TGGGGACAGT GGCTCCTACC 1980
ACTGAACAGA TGTCCTCTGC ACAGGTACTG TCCTCTTCAC CCAGCTGACC CATTTAGAAA 2040
GCTCAGTAAA TTAGGCTCAG CAGCCATGCA GGTCTGTGTG CCTTGCTCAG AGACCCCTAC 2100
ATGGCGTGGC CCCAGCCCCG TGCAGCACTT GTGACACTGT TTTAAAACTG CTGTTTCCTT 2160
GCCCACCTCC CCCATCTGGC CAGGAGTCCT CTGAGGACAA GGACCTCATT GTCTCCATCT 2220
TGGTATCACT GAGGTTCCAT CACAAGACCT GTCAGATGTG CAGTAGACAA ACCTAGAAGG 2280
CAGGCACAGC CAGAGCCAGA AAAGCCAGCT TTAGTCTGGA AGGAGCCACC TCATCCCAGA 2340
AGGAAGACCT AGTACCAGTG TCCATTCAGA AACTTGCTTC CTATCCACTA GCCTTCAAGG 2400
GTACCCTCCC TGCGCCCCAG GAGACAGCTG CCTAGTGTCC ACTGAGCCAT GGGCTTGGAG 2460
CAGAAGGAGC GAGCCAAGTC ATGGAGGAAG GGTGGGGGAG AGGGGAGTTC CCCTGACCAG 2520
AACCCTGTGG CCAAATGCAA ATGAGCAACT CAGAGCCAGC AGGCTCCAGG ACTGTGTATG 2580
GCAGGAGCTC ACAGGCCAGA AGAACTTGTC CCACCCTGAC AGATCTGAAA TGAGGGATGT 2640
TAAAATCTGC ATATTTGCAA GGTCCCCCTG 2670