Tag | Content |
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EnhancerAtlas ID | HS180-00669 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:20138790-20140520 |
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) |
NFIC | MA0161.2 | chr1:20139323-20139334 | TACTTGGCACA | + | 6.32 | NKX2-5 | MA0063.2 | chr1:20139083-20139093 | CTCAAGTGGT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:20138868-20138883 | TGAACTCCTGACCTC | - | 6.22 | SOX10 | MA0442.2 | chr1:20140485-20140496 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr1:20140485-20140495 | AAAACAAAGG | - | 6.02 | Zfx | MA0146.2 | chr1:20139812-20139826 | CCGGCTGAGGCCTG | + | 6.18 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28457 | chr1:20138630-20144503 | Fetal_Intestine | SE_29511 | chr1:20136289-20144541 | Fetal_Intestine_Large |
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Enhancer Sequence | GTGCCCACCA CCATGCCTGG TTAATTTTTT TGTATTTTCA GTAGAGATGG GGTTTCACCA 60 TGTTGGCCAG GCTGGTCTTG AACTCCTGAC CTCAAGTGAT CCGCCCGCCT CAGCCTCCCA 120 AAGTGTTGGG ATTACAGGCA TGAGCGACTG CGCCTGGCCT ATCATTTTCT TTTCTTTTCT 180 TTAGCATGGA TGACAGATTC TAAAATTCTC CGGCCTCTCT GAGCAGCTGA CTGCTGGAAT 240 TTGGAGGCTC CTGAAATTAG TTTCCTGTTC TCTCCATGCA CTTCTCAAAA ACCCTCAAGT 300 GGTGACCAGA TCCCCACTTA TTTGGGAGTT GTACACAAAG GAAGCAGCAT CATGAGGCAG 360 AAGGAGCCCT GGGTTATCTC GAGGGAGCTC AGGCATTGAC TGTGCAACCT TAGGCAGGCG 420 AATTCACCTC TGTGATCCTC AATCTCCTCC TCCGCAAGAG AGAGATAGTA ATGGCCTGTA 480 CTTCATAAGG TTATTGCGAA GATTAACTAG TGCATGGAAA GCAGTTATTG CAGTACTTGG 540 CACAGAGTAA GTACTGGATA AACAAGTAAC CACCATTATT ATGGTAGAAA TGGTGTCATT 600 AGCAACTGAA ACATTGGGGG GAGGTTTTGA TCTTGGCGAA GGGTCTGAGA AATATTACAG 660 ATCGAATAGA AGGGAAGTGA GTTGGGAGGG AATGTTCCTT GCCTATCCCA CTGGCAGCCA 720 TCCCAAACTG ACATGCCCGG GGCCAGCTCA GGAAATGCCC AGTGACCCTC TTCAGCTTGG 780 GAGACATGGT GTTCTTCAGG CCCACTTGGT CTGGCTTAAA GCCGTGGGTC TGTGCATGCC 840 CACACACACT CATACTGTCT CAGCACCAGT CGCCATTAGG GCCAATGGCA TGGGTGTCGG 900 ACTTGCCCTG AGACAACAGC ACTCCTCTGA GGTTTCAAGA ATGTTTCCCA TTTATGGGGC 960 TTTTGGAAGG AAATAGTATG TCTCCTCCCA TCCTCTGCTC ATCTGCACTC CCACATAAAC 1020 ACCCGGCTGA GGCCTGCCCC TGGCAACCAT GGAAAGTCGT TTCCCCCAGC CAATGCCTCC 1080 CCTGTGTTAA GAAGCAGACG TGGTGGAAAG AAGGCACGAA AAAAGCTTGC GACTCACAGG 1140 GTGAGGTGGG AAAAGTGGGG TTATTGGTGA GGACCGTTGC ATTTATGGGG CCTCTTATCT 1200 TTATGACAAA AGCTTAACTA GTACTTGAGA TGCAATAACA AAGACGGTAA CATCCATAAA 1260 GATCTAGTTC TACCGTGTGG GACTGTGCAA TAGATGGGCA GCTGGCCCCA CTGTATGTGG 1320 ACTGCAGTCC TTGTAACCCC GAGATTTGCT GCTAAGTCAG GGCCTAGTGG CACGGAGTGG 1380 GGAACTCCTA GTGAGGATAC TGGGAGCAAT TCCCAAACCC TGCCCTCTCC ACCCCTCCCC 1440 ATCTCTGCCA GCTAAATGTG GGACTCCCCC TGCAGCTTCA GAAACACCAT CCCTTCACAC 1500 ACATTTTGTC TCCCCAACCC TAGGGTCAAC TCCATGGGAG ACCTAAACAA CCAGGACACT 1560 TGCCGAGGCT AGGCTGGGCA TGAGATGCTC AGTGTTAGAG GAAGCGCAGT GGGACCTCCC 1620 CGTGGACTCC AAGCTCCCAG GAGGGAAAAT GTGTAACAAA GGGAAATGTG AACCAACTGC 1680 TGCCCCAAAC CCAAAAAAAC AAAGGAAAAC AAGAAAACAA AACCAGCTAC 1730
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