Tag | Content |
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EnhancerAtlas ID | HS180-44360 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr7:25901410-25902860 |
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) |
NFYA | MA0060.3 | chr7:25901798-25901809 | AGCCAATCAGA | + | 6.32 | NFYB | MA0502.1 | chr7:25901793-25901808 | ACACCAGCCAATCAG | + | 6.75 | ZNF263 | MA0528.1 | chr7:25902227-25902248 | GGAGGAAGGGCACGAGGAAGA | + | 6.14 | ZNF263 | MA0528.1 | chr7:25902224-25902245 | GGAGGAGGAAGGGCACGAGGA | + | 6.1 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00611 | chr7:25900935-25902267 | Adipose_Nuclei | SE_29953 | chr7:25892520-25903534 | Fetal_Muscle | SE_46258 | chr7:25900804-25902075 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I025860 | chr7 | 25899650 | 25902682 |
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Enhancer Sequence | GGTTCTAAAA CAAAATGGGA TATTAACCGT GTTTGTTTTC ACTTTGATCT ATAGGAAATA 60 GGTCCTGCAC CCTGTGACCC ATTAAACTAA TAAGATTATA CACATCAGCA GAGCGGAGGT 120 TCTAATTGTT TCCATCTGTC CCAGATCTTT GCATTTTAAA ATTGATGAAA ATAAGACATG 180 ATTTACAAAA AACAAAATAT ATTGAGAGTG AAAATGTGAC AAAAGTGAGC CCCTCGGACC 240 ACACATGCAA CCAATTACTG AGAAAATAAA TAGATGTATA TGGTGTGGCG CTTTTGGAAG 300 AAGAAAAACC GAAGCACGAA ACATAATCAT TGAATTGATC TGGGGGTACT CACTCATTTC 360 ATAAAGCTAA CACTTGCTTG AAAACACCAG CCAATCAGAA GCGTTTCCGG AAGACACTCT 420 ACACCTCTCC GCCTCTTCAT AAATATTTAA ACCGCTTCTT TCTAGATTTG TCATTTAAAT 480 CTACTAGGGA ATGTGCCTCA AGGGCTCATC TTTCACTGGG TCGCTCACAC AGAGGTGGGG 540 CGAGAGGGAG GAGGCGCATT AGCCCTGCGC TCTCATTTGC TTAAACGGCC TTCTTACGTC 600 ATCGTAAGCC TAAGCCAATC CGTGAAGTGC ACTTTGACAA GCTACCCGCC CCTAATTTGT 660 CCTTTCACCG CCAGCCTAAG CCAATAGTGT GGCTGCATGT AAATGAGAAA CCGCGAGCAT 720 CTCCCCCCGC CCCCGGCTCC GCCCAATTTC CCACCTCTTC CCGGAGCGCA CAGACGCCAG 780 CTGAGTGGGA GGGGCCTAGC TGCGGGCGGA GCACGGAGGA GGAAGGGCAC GAGGAAGAGG 840 CGGAGCGGGC CGAGGCGCGC GGAGCTGGGT TTGCTGAGTG CTTCCTTCCT CGGCCCCACC 900 TCCCGCCGGG CAGGATGCCG TTTGATCATT GGCTGGTTTA ATAAAGAGGG CGTGTTTATT 960 TTGCATAAAT AGTGGGCGGG CACCCAGGGC TGCTTTGTAA CTCGAGAACC CGGTGTCCCG 1020 CCTGTCTCCC GGGGGGTATG GGCGGGTCTC CCGCCAGCCT CGCCAGACTG AGCCAAGGGC 1080 CTGAAGGAAA TAAATGGCTT TCTGAAAAAA TTCGTCTTAA TTCGCCCTTT TGAGAGAATT 1140 CTGTTTCTAA ATGCATTTTT TTCGTTGGTT CTTACAAGTC GTTAAGAGTT GTAACATGAA 1200 ATAAGTAGAG ATCACCAATC TATCCGCCCC CAAATTAATT TTATTTTAAT CTGTGTAAGG 1260 GCCACTGCTC CTGGCTGGCC GTGTGTGAAG CAAAATTTTT GTGCAATAAA AATTATTCCT 1320 TCACTAGAAT TCATTTTTTC CTTTGCTATG AATTCCCTGT CTTCCTAATT TTCCACTAGC 1380 AGAGCTAGGG AGAGCCGAGT TGCACTGAAG CAGAGAAAGG ATGGAAAATT CTTTCGAGCT 1440 AAGCATTTAT 1450
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