Tag | Content |
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EnhancerAtlas ID | HS092-16289 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:65822370-65823530 |
Target genes | Number: 12 | Name | Ensembl ID |
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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) |
RUNX1 | MA0002.2 | chr14:65823431-65823442 | TTCTGTGGTTT | + | 6.32 | SREBF1 | MA0595.1 | chr14:65823480-65823490 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_43946 | chr14:65817761-65826181 | MM1S | SE_59685 | chr14:65748260-65827910 | Ly4 | SE_60978 | chr14:65748215-65845514 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I065351 | chr14 | 65818030 | 65824864 |
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Enhancer Sequence | TCCCCTCCCA GCCTTTCAAT CAGATTGCTG CCCCTAAACC CCTCCTACAG AGACATTCTG 60 ACTTCCAGGC ACCAACTGCT CCCCTAGACA CCAGCAACCT CCAGAGCCCT TTACAGAAAA 120 GGCGCAAGGC TCCAGACTCA TAGAATCCAA TTCTCTCTCT CATCCACAAA GCCCTAGCTT 180 CTCTCCAACC AATCCCCACC TCATCCTCTG GGGTACTGCC ATCTAATTCC TTCTTGGGTT 240 TGACCCTTGA ATTATAGAGA AACCATTAGC TAACTGCTGC CACCACTACC CCCAAGACAA 300 AATGAGGAAC TAAGACTGAC CGCTAAACAC AAAGCCTTAG CTAACTGGGG AGCTAGGAGG 360 TCAGTGAAGA GGAATAGAAT TTTTTCTTCC ACCGGGTGTA GTGGCTCACG CCTGTAATCT 420 TAGCACTTCG GGAGGCTGAA GTGGGTGGAT CACCTGAAGT CAGGAGTTCA AGACCAGCTT 480 GGCCAACATG GTGAAACCCC ATCTCTACTA AAAATACAAA AATTATCCAG CCATGGTGGT 540 AGATGCCTAT AAGCCCAGCT ACTCAGGAGG CTGAGGGAGG AGAATTGCTT GAACCTGGGA 600 GGCAGAGGTT GCAGTGAGCC AAGATTGCCT CATTGCACTC CAGACTGAGT GACAAGAGTG 660 AAATTCCATC TCAGAAAAAA AGAAAAGAAA AGAAAAATAT ATTTTTTTCT TTTTTTCCTA 720 TAGCAGAAAG GGAAAAAAAA AGCCTCATTC GATTATCATC ATTTGATGAT CGTTCTGTTA 780 CCAGCGTCAT TCCTTTGGGT GAGTCATTGC TGCCTCCAAG GGATCCCATA TTAGGATGCC 840 CCCTTGGGAG GGATAGGAAG CATGACTAAC ACCTGAGTAT AAAGAGGTTC ACCCTACACT 900 TCCTGACGTG GCAGGTGAGA GAGTGTGGGT GGGGAATTGG GAGGGGACTG CCTTTCCTTA 960 CTTTAGAGTC CTGTCCAATG GCTGGCTTTG TGGTTGGCTC CATTAGGGAG GGCCCACCAG 1020 GAAGCCTTCT CTTCTTTCCG TTGAAGACAA GCATGCAAGT TTTCTGTGGT TTGTTAGGGC 1080 TGGGCCACCA TGTCCTTAGT AGGCAGCAAG GTGGGGTGAT GACCTCTGAT ATCAAACCAT 1140 CTGGGAGTTA CTGCTGCTTT 1160
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