Tag | Content |
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EnhancerAtlas ID | HS180-02806 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:117013900-117016230 |
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) |
GFI1 | MA0038.2 | chr1:117015458-117015470 | CAAATCACTGCA | + | 7.22 | Hnf4a | MA0114.3 | chr1:117015191-117015207 | GAGGGCAAAGTCCTGT | + | 6.07 | Nkx2-5(var.2) | MA0503.1 | chr1:117015396-117015407 | CTTGAGTGCCT | - | 6.14 | RREB1 | MA0073.1 | chr1:117014694-117014714 | CCCCCCACCACCCCCCATCC | + | 7.75 | SPIC | MA0687.1 | chr1:117015285-117015299 | AAAAAGAGTAAGTA | + | 6.52 | Stat6 | MA0520.1 | chr1:117014435-117014450 | CCCTTCCTCAGAAGT | + | 6.01 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27848 | chr1:117013898-117021408 | Fetal_Intestine | SE_28774 | chr1:117013873-117021547 | Fetal_Intestine_Large | SE_50584 | chr1:117013866-117016332 | Sigmoid_Colon | SE_52493 | chr1:117013950-117016256 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I116471 | chr1 | 117014027 | 117021401 |
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Enhancer Sequence | TTAATTGCAT TAATTTTTAT TTATTAAAAT ATCAATTATT TTGATTGCTG AGTTTTTTCA 60 CTCTGCCCCC ACAGCTCCCG GACCTGGGGG CCCCCACCCC GTGAGCTCTG CCTTCCTGAT 120 ACACAGATTA CAGGGGAAAC TCAGACTCCC TCTGCAGGAG CTGGATGTCA GTTATCACCA 180 GGGCTCAGCT GCGTATCCCG AGGGCTCACT CTGCTTGCCT GATTCACCTC CCTTTCCAGT 240 TTTGCCTTCC CTTCTTCCTC TAGCAGTCTG AGCATTCTGC ACCTCCCCCT CCCTGTGCTT 300 CAATGCCATC TCACCCAACA TCCACACTAG GGCTGCATGT TCTCCAGAGC CTGCTCCATC 360 CTTCCCTTCC CTTCTACCCA CAACTGACTT GCTTTATAAT GGAAGAAGCG TTTTAATGCC 420 TGCCATGAAA TCCTGTCATC TGGACAGGAA GGGCAAGCTC CCTGGCTGAA TCATCAAGAG 480 GAGAGCACCT GCCTGGAATA AGGCTCTGAA TCTTCTACAG CTCTCTTTTC TGTTTCCCTT 540 CCTCAGAAGT ATCCCCTGGA CACCGCAGAG GCTGTAGAAC CAATACTGCC TGCACTGGCC 600 AACTGTGGGG GCAGTGGCTT CACACCCCGT GTGTGCTGCA AACACACTCA AATCTATGGC 660 CTGTAATAAT TTCTGCACAT CCCTGTGTTG CTCCCATAGG ACAGATAGAG GCACAAAGGC 720 CCTGGCTGAT AAGTCGCATC AACTGATCAC ATAACCACTC ATTGACAAAA CAGAGATTAA 780 ACCTATATTT TTGACCCCCC ACCACCCCCC ATCCTGTGTC CATTTCATTA TTCCATAAAC 840 ATTCCCCTCT ACCACACCCT ACTTCCCCCT CACCTGCCCA CCCCTGCAAA GTCACTTGAT 900 CTCTTGGTGA ATTAGCATGA GCCAACATTG ATGTTTTAAA ATAGCAAATT TTCAGGCTGA 960 AAAAAGTCAA GATCATCTTT AAGTCCCCAA GGACATATGC AACCAGTGAT AGAAAAATCC 1020 TCTCCCACTT CTCCCCCTCC AGTCTGAATT GACTTAGCAA CTTTTCTTCA GCTCCTCAGC 1080 AGAGCCTTTC ACAAATTCCC ACTTGCAGCA CTGCTGAAGG ATAGACATCC TGATGTGCTC 1140 TCAGCTGGAC TGCTGCTGTG GGCTTCAAAA AAACAGATGC AGCAGCAGTG AGTGTGTGCC 1200 TGTATTATAT TTCTCAAGTG AACATCTTCA GAAGCTGGGG ACATGTGTTT TCTAGCCCAG 1260 CATGTAGGAT CTGTGGCCCC TGAGGCTGTG GGAGGGCAAA GTCCTGTAGA GAAGCTATTG 1320 TTTTCCTTGC CTTTGCTGAT AGCATGAGAT CAGCTAAATG ATGGTGGCAG GTATCCAAGA 1380 CCAAGAAAAA GAGTAAGTAG GGGTACAGTA ATGGGAAGCA GTAAATCGTA GGACATATTT 1440 GTAATCTAAG CAACAAAAAT CAAGCATTCT CTGGGAAATG CATGAAGCAC TGAATGCTTG 1500 AGTGCCTAAT GGGTTTTGAA GCCTCAGTAA GTTTATGTGG ATGGGTGCCA AGAGCAAACA 1560 AATCACTGCA GCCACAAGCT GCCTCACTCC ATATCCGAGA TGCATACTGA GAATGACTGG 1620 GAAGGCTACT TGGTATGGGA ACCCTAAAGC AGTTAGGATG GGGAGGCCCC CGGGGAAATG 1680 CTATCCTTAG TGCTCTCCAG GAAGCATCAT TTACAACTTC ACCATTGGCC AAACACTAAT 1740 ATATGTGCTT TACATATATC ATCTCATCGA AGCCTCATTA TAACACTAAT GGGTTAGGTG 1800 TTATTACACC CCTATTTTAA AGATGAAGGA AGTCAGACTC AGTTAAGATC ATACATCTAT 1860 TAAGAGGTAG GGCAAAATCC AGACTCAGTC TTTTCTGATT CCAAAGCACC TGCTCTTAAC 1920 TGCCCCACTT TATTGCCCTC AGAGCTCTTT GGTACCAATT ACACCAGGCA TTCCTAGCTA 1980 CAAGGCATTG TTCATTCATT CATCCATTCA TTCAACATCC AGCAATATTT CTTGAGCATC 2040 TGCATCGTGC CAGGCCCTTT GCTAGGCCCT GGGACCTCAC TGATGAAGGA GACATGGACC 2100 CTGTCCTCAT GGAACTTGGA ATCTAATGAG TGAGTGCCAG GGTCTGGAAT GGGAGTTAAG 2160 GACTCACTTA AGACTGGGCA GGTTGTATCT TGCACAAAGG CTCTGCACTA AGGGGGCAAG 2220 TGGGTACTGA AACCCAGCTT ATATTCCACT AAGCTATGTG CCCACAGAGC GACATCTTCT 2280 AGAGGAAGCA ATTTAAAAAA TTTTTTCCCA AAGAGTAATA TGGGCTATTC 2330
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