Tag | Content |
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EnhancerAtlas ID | HS092-15286 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr13:110758640-110759670 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG2 | MA0669.1 | chr13:110758707-110758717 | GACATATGTT | - | 6.02 | STAT3 | MA0144.2 | chr13:110758876-110758887 | TTTCTGGGAAG | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41265 | chr13:110758693-110763089 | Left_Ventricle |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I110106 | chr13 | 110759166 | 110759376 |
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Enhancer Sequence | TTATCAGCAC CTCTCATTCA TTTCACATGC AAGCCAGCTT CTTAGAGGAA ACAGCATTAA 60 TTATGTAGAC ATATGTTTAT GTTGGTCAAT GGACTTCTTG CTGTTGTTAT ATGGCTTGAG 120 GATTGGTCTC CTCTTTTACG ACAATAGTCA TAGAAAATGT TTCACAAGTA TATTACAGAA 180 GTGACAGCAT ATATCAAAGA CACTCCGTTA AAGATGAAAG TGTAGAAACG CCAGGTTTTC 240 TGGGAAGGGG TCGCCCAAGG GAAAGAGTTG AAGATTGAAG GTTGATAGGA ACAGCCTGTG 300 TTCAAAGACA GTCATGAGTT TACGAAGCTG TGGAATGTTT ATGGAGGACA TCGGCCATCC 360 AACATGAGGA TGAACTTCAT TCCCCGAGGC CTGGCGCAGG ATGGAGCTGT GATTACGTGG 420 GCTGTCCTTT GCACGGGAAC AGGGGCTCCA TCGATGAATA ACAGGGGGTA CCTCCAAAAG 480 GCCACGCTGA CTCTGGGAAT TGCTTTGAAT TTCAGGCTTA GAGAGCTGGG GCTGGAGTGC 540 TGACCATGAC TTTGAAGCTA AAAGCAGTGT GTGCTCTGAG GCAAGGAGCT GCAGCTTGGA 600 CCTGAGCCCT GGGAAGCTGC CCAGAGGCAC TGCATGGCAG AGCAGGCTGG GGGCAGGAGC 660 AGAGACAGCT CTTTACCGAG ACCAGCTCCA AGACAGCTCG CCCCTAATAA GGAAGTAGAG 720 TGGCACTCCC CCATACCTCA TCTCAGAGAC CTCCCAGGTC CTTCAGCCTC GCTGAAGGAA 780 GGCCGAGCCT CTGTGGGGCC CTGAGATGTT AGGGCTGAGC AGATTCTAAA GCAGGACTCT 840 CAGTCCTGAG CAGCAGAAGA TCAGATGAGG GTGAGAACTG CCCCCAAACT GAGCTGCCAG 900 TTAGATTCAG AAATGTGCTC AGGCTGGTGG GTAGAGCTGC CTGACACTTT ATTCCTTTTC 960 TTCATGTCAT TTACTGTAAT ATTAATAATC TCTGGTTACA CATCATCTCT AAATGTCACG 1020 ATCTTGAAGG 1030
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