Tag | Content |
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EnhancerAtlas ID | HS177-13403 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr2:235909150-235910420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr2:235909591-235909606 | TGGACTTTGCTCTCA | - | 6.41 | Mecom | MA0029.1 | chr2:235910047-235910061 | GAGATAAGATAAGC | + | 6.7 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_29217 | chr2:235906866-235919843 | Fetal_Intestine_Large | SE_31459 | chr2:235906623-235912907 | Gastric | SE_35323 | chr2:235906721-235910668 | HepG2 | SE_47184 | chr2:235907005-235910190 | Panc1 | SE_47485 | chr2:235908379-235910243 | Pancreas | SE_47485 | chr2:235910267-235910538 | Pancreas | SE_53059 | chr2:235906751-235910643 | Small_Intestine | SE_65336 | chr2:235908160-235910108 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I234998 | chr2 | 235906788 | 235921345 |
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Enhancer Sequence | CCCTCCTTCC AAGAGGGGCT TAGCCAGAAG GGGAAGCCTG GATCTTGGGC TCGGGCTCTG 60 ATGCTTTGTC TCTGAGCCGC TGACATGGAG GACGTCAAGC CGCGATGTTC ATGTCCCCAT 120 TGCGTAGAGG TGGGTCCTGT AGTCCCACAT GTGGTGTGCT CTGAATCTCC TTTCCACTCT 180 GTTGGAGGGT CAGAGGGACT TGAAAGATCA CAGAGCCCAG CCTCGCATTT GGCAGAAGAG 240 AAAGCAGAGA CATAAAGGCC AGGGACTTGT GCCGGGTCCT ACCCGCTATC TGGTGCCCCA 300 CACACTGGGG CCTGTCCCCA CTGCCAGCAG CCTCTGTGTG GGTTCTGCCT TTTTCTGCAC 360 TGGTGGTGTC TCCCCATCGC CCCAGCTGCT TGTGGGCAGG CGTCACCTTG TTCTGACCTC 420 TTTCCTTCCC CCAGGCAGCT CTGGACTTTG CTCTCAGTAA ACACAACTTG ATTCTTTTCC 480 TTCTTACCTT ATCATTGCCC ATAAATCCCG TTTACACGGT GCCCACTTTT GTGTCTGAGC 540 TGGGACGTAC AACCTCGTCT CTGCCTCCAG TTTTTGAGAA ATTAATTATA AACAGTGTTG 600 ACAGAGGCTC TGGCTTGACT TGGGGCATCT GCTGCTCTTC CCGGCCTTGG TCTTCTGAAG 660 GTAGCTGTTA TCAGTAACAG AACAGATGTG TTTATCCTGG GCTCCCGGGC CCTTGGCGTG 720 GCCCTTTGAG GGGGTCTGTG AAACCCCTGA AACTGCATGC TAAACTTTAC GGGTGGAGGT 780 AGTTTTCTAA AGAGAGGGTC CAGAGACTTT GTCAGATTCC TTAGAGGATT TGCACCCTCA 840 AAAAACGTTA ACAACCTCTG AGCTGGAGGA AGGCCTAAGA CAAGCCTATC GCACTTGGAG 900 ATAAGATAAG CCGAGGCGGG ACCTAATGGG GCCTCAATGT CTTGGCCAGA GTGCACAGCT 960 GAAACGGAGA TGACACTTGA CAGAAACCAG TGTAAAACTC TCCTTCCCTT TATTTAGCTT 1020 TTATTTCTTG TGCTTTTCAT TAAGTACAGA TACTCTTTGC TTGCTTACAG AACAGGGAAG 1080 ACCTGGCTTC TGAAAATTAT CTTTAGGTTT TTCATTGAAT TTGGTCTTAT TCTGAACAAT 1140 GCCTGAACGT CGAAGGTGCT CCCCTAGATA GGTTAATAGA AACCCACAGT CCAGGGCAAG 1200 AGGCCGCATC CGGGAAGCCT GTGTACAGGT GACTGGAGAG ATGAGTTCTC ACGGACCGTT 1260 CGGGCAACTT 1270
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