Tag | Content |
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EnhancerAtlas ID | HS044-10681 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:131723100-131724610 |
Target genes | |
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) |
JUN(var.2) | MA0489.1 | chr5:131723448-131723462 | ATGACTCATTTCTT | - | 7.12 | RARA(var.2) | MA0730.1 | chr5:131723962-131723979 | TGACCTTTTGTTGAACT | - | 7.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_25154 | chr5:131722248-131724802 | Colon_Crypt_3 | SE_26597 | chr5:131723314-131726622 | Esophagus | SE_54554 | chr5:131720956-131726150 | Stomach_Smooth_Muscle | SE_62219 | chr5:131721125-131837948 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I132384 | chr5 | 131720053 | 131726700 |
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Enhancer Sequence | GCAATCATAT ATTTTAACCA TTACTTCTAA CAATAAATAC TCTTTTTGAG TAATAGGCCT 60 TTCATAAAGT CAGCATTTGG GAAAATCATT GTTTCTTATA CCTAAGGTGG CTTGTCACCT 120 TACAAAGCTA ACCCCAAACG TAAAATGTAA AGCACAAATA GATTTGGAGT TAGAAGTATT 180 TCATCTCTTG AGTATTAGCA ATTATTCATT AAAAAGAAAA AAAAAGTGTT TAGTCTCTTT 240 CTGCCCTCCA ATGGTTAATT ATTGCATATC ATCTTGGAGT CAGGTCCTTT TTGATGTCCA 300 CCTCTTCCCC CTACCCCACC CCTCCCGTCA GCCCTGTTCT CACACACCAT GACTCATTTC 360 TTGGCTCTAC CTAGTTCCTG GTTCTTGCTT TTCCTTCCCG TTCCCTCTCC TACCATCTCT 420 GTAGCAGGCA GTTTTCCTTG GTCTCGTGAC TATGAGAGGT TAGAAGCTGT AAATGCTGCC 480 TGGTGGGGTT CTGGAATGTG TCTGTGGTCT GACTGGAAGA TGAGGGGTTG GGTGTGGGAA 540 CAGCCACAAG CAGCCCTGCT GAAGTGTGAG AGGCAGGCAT GGTTGGGCTT GGAAAAGAGG 600 GAACAGTTAT TGTAGACAGC GGAGGCCAAT GGCCACTGCC AGCCCTGCAG ACTTCCCAGT 660 GAGTGGTGGC CCAGCAGCCA CTGTCAGCAT GCACCAGAAA GGGGTCCTGT GCGCAAAGGT 720 CAGGCAGGAG TGTGGCAGAG GGCTTTTAAG TTAGGTGGTT TTGGGGGCTT TTAAGTGAGG 780 GGTCAATCTG GGTGAATGCA TAAGCCCCAC TGGCATCTTT GAGGAAATGA GGCTATTTCA 840 GGGGATACTT TCAGTCCAAA GTTGACCTTT TGTTGAACTT CTAACTCTGG AAAAACAAGC 900 TCCAAACCTG GGTTTGCTTA AGAAAGCAAC ATCAGTGTGT TTAGACGTGT GGTTTATTAA 960 TGGCCTTGGC TGTGCTGAAT TTCATAGGAA GTCACTCTGG GTGAAGCTCA GGTCAATTTT 1020 CCTGTTTTTC TATTTGAATT CTTTTTCCCT GGAAGCACAC CAGTAACTAC ATAGTATAAG 1080 GACTCAAAAC ATTAACTTTT AAAAAATATC AGACCAATAA ACCACACAGC CAGGTACTCT 1140 CTCTGACCCA GAGGGCAGGG AGCCAGGCTT CGGGAGGAAT ACTTAGAGGC CTCCTTGGAA 1200 TGTGGCCACC GACAGGAATA TGTGGGGGTG CAGTGAGGAA GCTGTCAGCC TGGGCCTCTG 1260 TCTTCCTGTA CCCTTGAGGG ACTGGTCACT TACTTTTCCT CATTTTCATT CACTCTGATT 1320 TGTTACTGAC AAGGCCTAGG GAAGTTTTCA CAGCCTAAAA CACAGTCAGT ATACTTACTG 1380 TTCTTAGAAA CGTAACACTC CCCGACGCTG AGATGCAGAC AGCTAAGATG CCAGGGATTC 1440 AAGTATGTTA TTGTGTGCTC TGAGTCTCTG ACCACCTCTT CTTCCCATAC ACTTATGATG 1500 TTGTTCCTGC 1510
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