Tag | Content |
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EnhancerAtlas ID | HS030-02249 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:214149880-214151270 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:214150442-214150457 | GGTTAATTATTGACT | + | 6.07 | HNF1A | MA0046.2 | chr1:214150442-214150457 | GGTTAATTATTGACT | - | 6.68 | HNF1B | MA0153.2 | chr1:214150443-214150456 | GTTAATTATTGAC | - | 6.25 | HNF1B | MA0153.2 | chr1:214150443-214150456 | GTTAATTATTGAC | + | 6.41 | ZNF263 | MA0528.1 | chr1:214151057-214151078 | GGGGGAGGGGGAAAGTGGGAG | + | 6.52 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_65842 | chr1:214150319-214151482 | Pancreatic_islets | SE_68033 | chr1:214146367-214176127 | TC32 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I213976 | chr1 | 214150320 | 214150779 | GH01I213977 | chr1 | 214150941 | 214151090 |
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Enhancer Sequence | TACTTATTTG AAATTCAAAA ATAATTTTCA TGCTTTGATA GGAATGTGCG GTTGTTTATC 60 ATTTCAAAAG CACTTCTCCT TTTATCACGA ATCGAAGAAG AACTAACATT GAGAAACAAG 120 GAACCAGAAT ATTTAGAGAT GCTGGGAATA AACTACAAAC TAACATGGTC AAGGGAGAGA 180 AAATATGATC CTCTCAGAAG AATAATGTAA CAACAATCAG AGCACATCTG GGATTTGATT 240 CAAACCAACC TGGAACCAGA TTGGATCTCC AAGCTGTTCT GTGTATACAC ACACACACAC 300 ACACACACAC ACACAGACAC ACACGCTGAG ATTTCCAAAA GTGAAATTTC CAGAAGTTAT 360 CCTACAGAGT TAACCCCAGA AAGGACTTCA CTGGCAGACA CAGGCATAAC TTTACTCCTT 420 TTGTGATGAC CCATGAGTGG GGTCTATGGC AGTCTGAATA GATGGGCCTT TCTGTTGAAA 480 GATTCTGCCT AATCCTTCCC ACCAAAGCAG GGTTCTAAAG GTGTCAGCAG GATTTGGCTG 540 ACTGGATCGT TAATGGAGCT ATGGTTAATT ATTGACTGAT TAGGGATTTA CCTTATCTTT 600 CCGTCAGGAG CTGGCTCAAG ACTTAACGGT AAGCAATTTA GAGCCAGGGT GAACCTACAC 660 ACATGCCTTT TTCTTCTTTT CCTTTGGGTC ACTTTAGCTT GCCCCTCCCC ATAATTCACA 720 TTCAGGACAG AATGGCCAGT CCTTACAAGG CGTGGGAGTC CTCAAGAGCA CCGAAAATGA 780 GAGGGGCCAG GTCCACGTGA CAAGTGTCCA GAGACAGAGG CTTAGAGAAA TGTGCCTTTT 840 GCAAAACAGT GTTTATGTGT AAAGGTTTTC CAGTTAAGTC CCTGGGAGAA AAAAAAAAAA 900 AAGCACTTGC TTTTTGTCTC TAAAAGGTCT GGTGATGCCC GTGGGTGAGA ATCCACCCCG 960 CACTCCCCAA GGCCCCTTGG CAAAGCCAGG GAATGAGTAC AGGCAGCTCA GGCCCAGCTG 1020 CCCCAGATAA GAGGTGGCCC GTGTTAATGC ACAGGCTTCC TCTGCACCTC AGCAGGGCCT 1080 TCCTTTTCTA AACAGTCTCC CTTTAATGTT GGCGAATGTT GTTTTTCCAT TGACTCAACA 1140 TCTCGCCTGG TGGTAAGCCA GTGAGGAAAG TTGCAGCGGG GGAGGGGGAA AGTGGGAGAG 1200 AGTGATGCCA AAGCAAAAGA GCGGGACGGT CAGCCAGGTT TCCAAACAAG CTAGACACCT 1260 GCTTTGGAAA GACAGTGACC AAGCCTAGAC TTCTGGCTTC CTCTTCACTT TGATCAGCCT 1320 TTTGTTCCCT GCGGGTCTGT GATGGGCTCC CTGCCCCTCC CCTCACCACT GCCCCCTTCA 1380 CTGGGAGCTA 1390
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