Tag | Content |
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EnhancerAtlas ID | HS108-12547 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:93789110-93790730 |
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 | chr14:93789622-93789637 | TGTTAATGTTTAATT | - | 6.48 | Nfe2l2 | MA0150.2 | chr14:93789745-93789760 | AACTATGACTCTGCA | + | 6.01 | ZNF263 | MA0528.1 | chr14:93789690-93789711 | TCTTCTTCCCCATCCTTCCTC | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28433 | chr14:93788943-93791090 | Fetal_Intestine | SE_28901 | chr14:93788438-93791464 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I093322 | chr14 | 93789062 | 93791187 |
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Enhancer Sequence | ACACAGTATC ATATATTTTT AAAGGTATAC TCTATTCCTC TTGTCTTCAT TTTAAAAATA 60 ACTACAAGGC TGGGTGATGT GGCTCATGCC TATAATTCCA GTGCTTTGGG AAGCCAAGAT 120 GGGATGAATT GCTTGAGGCC AGGAGTTCAA GACCAGCCTG GGCAACAACA CAGCAGGACC 180 CCATCTCTAC AAAAAAAAAT GTTTACAAAT TAGCTGAGCA TGATGGCGTG TGCCTGCTGC 240 CCTAGCTACT CAGGTGGCTG AGGCAGGACA ATCTCTTGAG CCTATGAGTT TGAGGCTGCG 300 GTGAGCTATG ATAGGGCCAC TGCACTCCAG CCTGGGCACA GAATGAGTAT CCTGTCTCTT 360 AAAAAAAACA AACACTGCAA AGCTGGGTGT GGCAATCTCA ATTACTCAGA AGGCTTGAGG 420 ATCGCTTGAG CCCAGGAGTT TGGAACCAGC CTGGGGAACA TAGCAAGAAC GCGAATAGAA 480 AAAAAAAATT TTTTTAACCC TACAAATTAC TATGTTAATG TTTAATTTAT TTGACCAAAG 540 CCAATAAATG ATGAAATATA TACAGTTAGT AAATTGTAAC TCTTCTTCCC CATCCTTCCT 600 CCCTTATCAG ACATTATTGT TGAAGCATGT GACAGAACTA TGACTCTGCA ATTGAGGCTA 660 TGAGACTTCT GTCATAGCTA TCACTAACAT TCACTACAAA CTCATCCAGT CCTGTCACAA 720 AGCTTTCTGC TTACAAGAAA ATTCTCATGT CTGGTCTTAA GCAAGCAAAA AATATTTTAG 780 GCAAGTCTGA AGACAAGAAT AGGTCTCATG AAGCATATTA TAGAATTTTT CTCTAAAGAA 840 TAATTCACAA TTGAATCCCA GATGAAACAG AGCTAAATGT AATATTGCTC CTTCCGTAAA 900 GGACTACAGC CAGGAGACTG ACATAGTTTT TATCTAAATG AAAATGTCTA GGTAATAATG 960 AGGGGCAAGC AAAAAACAAT GTCTGATCTC ACTGGTTTTT CCATTTTTAC TTTAAAGACA 1020 ACACCACACG TCATGTTTAT TTAAAAAATG GCTTACAATT AGCAGAACAG AAACTCTTTA 1080 AAAAACTGCT TTCAAAGCAC TCTTTCATGT TACTATTTCA TCTTAACTCA CTTACTGAAT 1140 ACCTATTACT TGTTGTGTGA CACTATTAGA CACTGTGCGA CATCCCGTAC ACTTTGGTTC 1200 AAACCATACA GTCATGTAGA GGAGTCAGGC ATACAAGCAA TTATAATACA GGGCAATAAA 1260 GAATAGAAGT GTAAAGTTCT AAAAGAACAT ATGACTATTG TGCAAAGTTC CAAAAGAATG 1320 TATGACTGTT GGTAAAGGTA TCATAACTTG ATCTTGAAAA ATAAAGAGGA CTGTATCAAT 1380 CAAGAGATTT TGGGCCAGGT GCAGTGGTTC ACACCTGTAA TCCCAACACT TTGGGAGACT 1440 GAGGTGGGAG GATCACTTGA GACCAGGAGT TCAAGACGCC TGGGCAATAC AGGGAGACCC 1500 TGCCTCTACA AATAATTTTT TTAAAGTAGC CAGGTGTGGT GGCTACTTCT CAGAAGCCTG 1560 AAGCAGGAGG ACTGCTGAAC CCAAGAGGTC AAGGTTGGAG TGAGCTGTGA TTGTATCACT 1620
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