Tag | Content |
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EnhancerAtlas ID | HS190-00061 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:8958910-8961000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:8960846-8960856 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:8960846-8960856 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:8960292-8960307 | GAGGTCAGGAGTTCA | + | 6.22 | Nr5a2 | MA0505.1 | chr1:8960300-8960315 | GAGTTCAAGGACAGC | + | 7.06 | RARA | MA0729.1 | chr1:8960292-8960310 | GAGGTCAGGAGTTCAAGG | + | 6.73 | STAT1 | MA0137.3 | chr1:8960153-8960164 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr1:8960153-8960167 | TTTCCAGGAAAGGG | + | 7.64 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_27088 | chr1:8959478-8960765 | Esophagus | SE_34103 | chr1:8959575-8960842 | HCC1954 | SE_34433 | chr1:8958839-8961107 | HCT-116 | SE_34916 | chr1:8959109-8961267 | HeLa | SE_36553 | chr1:8959977-8960884 | HMEC | SE_46612 | chr1:8959902-8960819 | Osteoblasts | SE_47312 | chr1:8959436-8960657 | Panc1 | SE_56056 | chr1:8958921-8961024 | u87 | SE_67633 | chr1:8958921-8961024 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I008899 | chr1 | 8959185 | 8960724 |
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Enhancer Sequence | CACTGGGAGG AACAAACAAT TCTGGACGCG CCACGTTTAA GAGCTGTAAC ACTCACTGCG 60 AAGGTCTGTG GCTTCACTCC TGAAGTCAGC GAGACCACGA ACCCACCGGA AGGAAGAAAC 120 TCCGGACACA TCTGAACATC TGAAGGAATA AACTCTGGAC AAACCATCTT TAAGAGCTGT 180 AACAATCACC GCAAGGGTCC ACAGCTTCAT TCTTGAAGTC AGCGAGACCA GGAACCCACC 240 GGAAAGAATA AATTCCGGAC ACAACATTTC TTTTTTCTTT GAGACAGGGT CTCAGTGGCA 300 CAATCATAGC TCACTGCAGC CTCAACCTCC TGGGCTCAAG AGATCCTCCT GCCTCAGTCT 360 CCTGAGTAGC TGGCACACCG CCATGCCCTG CCAATTTTTT TTGTAGAGAC AGGGGTCTCA 420 CTGTGCTGCC TACACTGGTC TCGAGCTCCT GGTCTCAAGC AGTCCTCCCT CCTGGTCGTC 480 CCAAAGTGCT GGGATTATAG GTGTGAGCCA CCGTGCCTGG CCTCTTTTCT TCTTTTTTCC 540 CTCCACATGT GTCTTATTTT TTTTATTTTT TTATTTTTTG AGACAAAGTC TTGCTCTTCT 600 CCCCCAGGCT GGAATGCAGT GTTGCCATCT TGGCTCACTG CAACCTCTGT CTCCCGGATT 660 CAAGCAATTC TCCTGCTTCG CCCCCTCAAG TAGCTGGGAT TACAGGTGCC CACCACCACG 720 CGTGGCTAAT TTTTGTATTT TTAGTAGAAG CGGGGTTTCA CCATGTTGGC CAGGCTGGTC 780 TAGAACTCCT GACCTCAGGT GATCTACCCG TTTCGGCCTC CTGAAGTACT GGGATTAGAG 840 GCATGAGCCA CCGTGCCCGG CCGTCTTTTG CTTTATTTTT GAGACAGAGT CTCACTCTGC 900 TGCCCAGGCT GGAGTGCAGT GGTGCTATCT CGGCTCACTG CAACCTCTGC CTCCCCGGTT 960 CCAGTGATTT TTGTGCCTCA GCCTCCCGAG TAGCTGCTGT GATTACTACA GGTGCCCACC 1020 ACCACGCCTG GCTAATTTTT GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGCTCAGG 1080 TTTGTCTCAA ACTCCTGGCC CCAGGTGATC TGCCTGCCTT GGCCTCCCAA AGTGCTGGGA 1140 TTACAGGCAT GAGCCACTGA GCCTGGCCTC TATATAAGCC CTAAGTTCTA ACCGCTCCTC 1200 TGAGTTACTC ATCACTGAAT TTCCGTTGCA GGTGATTCAT GAGTTTCCAG GAAAGGGGTG 1260 GGTGATTTCC AGAATGAGGG TTCCTCCCCT TTTTAGACTA TATAGGTAAA CTTCTGGGCC 1320 AGGCATGGTG GCTCATGCCT GTAATCTCAG CACTTTGGAA GGCCAAGGCT GGCAGATCAC 1380 TTGAGGTCAG GAGTTCAAGG ACAGCCTGGC AAGCATGGAG AAATCCTGTC TCTACTAAAA 1440 ATACAAAAAT TAGCTGGGCG TGATGATGTG CTCCTGTACT CCCAGTTACT CAGGCAGCTG 1500 AGGCAGGAGA AGCCGGAGGC AGAGGTTGTG GTGAGCCAAG ATTGTGCCAC TGCACTCCAG 1560 CCTGGGTGAC AGAGCAAGAC CCTGTCTCAA TAAACTAAAC TAAACTAAAA TAAATAAATA 1620 AAGGAATAGA CTACATAGGC TAACTTCTGG ATGTGGCTGT GGCATTTGTA AACTGTCATG 1680 GCGCTGATGA GAGTGTCTTT TAGCATGCTA ATGTATTATA ATTAATGTAT ACTGAGTAGG 1740 GAGGACTACC AGAGGTCACT TTCATTGCCA TCTTGGTTTT GGCTGGTTTG GGCTGAGTTC 1800 TTTTTTTTTT TTTGAGACAG AGTCTCACTC TGTCACCCAG GCTGGAGTGC AGTGGCACAG 1860 TCTCAGCTCA CTGCAATCTC CACCTCCCAG GTTCAAGTAA TTCTCCTGCC TCAGCCTCCT 1920 GAGTAGCTGG GATACAGGCA CGTGCCACCA CACCCAGCTA ATTTTTGTAT ATTTAGTAGA 1980 GACGGGGTTT CACCATGTTG ATCAGGCTGG TCTCGACCTC CTGACCTTGT GGTCTGCCTG 2040 CCTTGGCCTC CCAAAGTCCT GGGATTACAG GCATGAGCCA CCGCACCTGT 2090
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