Tag | Content |
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EnhancerAtlas ID | HS048-33986 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr7:65821850-65822830 |
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) |
Foxd3 | MA0041.1 | chr7:65822402-65822414 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr7:65822406-65822418 | GTTTGTTTGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_36384 | chr7:65816602-65823087 | HMEC |
|
| Number: 1 | ID | Chromosome | Start | End |
GH07I066351 | chr7 | 65816876 | 65823018 |
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Enhancer Sequence | TACATGAGGT GAGGGTTGGG GGACATTGCC AGGTCTTTCT GTTTCCCACT CGGGCTCTTG 60 CAGGGGGCTG GGTGGCCAAG GTGGAGAGCA CAGCTCTGGA GTCCGTCTGC CAGGGTTGGA 120 ATCCTGCCTC TTCACTTTCT GTGTGGAAGC AAGCACATTA CTTCACCTCT CTGTGTCTTC 180 ATTTATTCAT CTATGAAATG AGGATAATAT TAACAAGAGC ATGGTGGTGA GAATTAATCA 240 TCATCCAAGA GCCTGGCTCA TAATAAGCGC ACAATAGTAT TGTTATTTTC ATTATGAACC 300 ATGAAATATT TCAGCTGAAA GGGACCTGGA GGCCATCAAG CCCAACTCCC TGTTTACTGA 360 TAAGGAAGCT GGTCCCAGAG GGAGCAGGTC GTTTGTCAGG ACCATAGTCC ATAGGCAAGG 420 AAACCCAGAA CTCAAGAGTG GCTGTTTACT TCTGGTTACC TGTTCAGCCA GGGCCCCAGC 480 CACCCATCCC CACCTCCAGT GGCTTTCTTC GTGTGCTGGA CTTGCAGATG TTTTTGCCCT 540 ACTGCAATTT TTGTTTGTTT GTTTGTTTCT TGGTTGGTTT TTCAAGTTTG CCCTTGCTTG 600 TTTTAATGTA TTATGGATGG CTTATGTGAG TAACCTATAT TGTCTCATTG GACTAAGTGC 660 TACATTGTAG ACAAGGCCAG CCTTGCCTTC TCAGCCCTTT TTCTATCTGA GTATGTGGCC 720 CTCATCAGGC ACATGTCCAG GGACACCAGC TCATGAGTGG CAAAGCTGGT TTCTCAGCCC 780 AGATCTCCAG GTGCAGCTGC TCAGAGTTCA TACCCTTGTC CCAGACTTTC AGTCTCTGCT 840 TATCCACCCA AACTTTCTTA AGATCAGTTT TGCTCCAAAT GATGTGGCAA AGCCTTTGAT 900 CAGTTGTAAC TTGAACAGCC TTTTCAAAAA ATCTGATATT GGCTGGGCAT GGTGGCTCAT 960 GCCTGTAATC CCAGCACTTT 980
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