Tag | Content |
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EnhancerAtlas ID | HS180-04312 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:207141810-207143430 |
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) |
MAFG | MA0659.1 | chr1:207142524-207142545 | TAAGTGCTGATGCAGCACATG | + | 6.1 | PROP1 | MA0715.1 | chr1:207142443-207142454 | TAATTTGATTA | - | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23166 | chr1:207141832-207143705 | Colon_Crypt_1 | SE_24017 | chr1:207141819-207142508 | Colon_Crypt_2 | SE_24017 | chr1:207142691-207143558 | Colon_Crypt_2 | SE_26377 | chr1:207140549-207143554 | Duodenum_Smooth_Muscle | SE_28474 | chr1:207140000-207149527 | Fetal_Intestine | SE_29373 | chr1:207139921-207149527 | Fetal_Intestine_Large | SE_58988 | chr1:207121014-207154864 | Ly3 |
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Enhancer Sequence | GACCTATAGA TTTTTGAAAA AGCAAACTAA AGTTAGCCGT TGAGTTTTTC TTCCTACTCT 60 AATACGTTCC TCACTACTGT TAAGGACAGG CGCTAACAGT CAATGGTTTG GCCCATGGGC 120 AGAAACCCCC TCACTCCCCA AACAGTTTAA GCCATGCAAA ACCACTGGCC AGTTTGTGAC 180 ACAGGCTGTG CAGGAGGGAA TCACAAAGAG GAAAACAGGG AATAGGGGAA AAGAGAAGGC 240 AGAGGAAGTA GGAGAACAGG GAGAGAAAAG GAGAGGTAGG AGGTGAAAGA AGGGAAAAGG 300 GAAGAGAGAA GACAGAAGCA GAGAAAAGTA GAGAGTCCAT GGGGTGGCCC TGAGCTTGTT 360 TTCCTGCAAC TAGACTTGGC AAGTTGTCCC CTCAGCTTGG CTCTGCCCAG CCCTCTCCAC 420 TAAGGCCTTT CCCTGCTCTA CCCAGTTTGA GCCCCAAGAA TGGCCAGATC TTTAAAAGTC 480 CATAGGCTCT TTATGCATCT TTCTGTGCCT TCGCTGTAGC AAGTCCCCTA GCTTGGGCAC 540 TGCGATGGCA GTCTCAGACC TTTCCCTGCC TTACAAAGCT TCCTGTCCCC ACCTGGAGAC 600 TCTCCCAGGG TGTTTGTTCC TGCACCTAAC TCATAATTTG ATTAATATTC ACCAAGTCCT 660 GGCTGATTCT GGGGCTGGTA CCTAGACTCC CCCGGGTGAA TTTTTCTAAA GCACTAAGTG 720 CTGATGCAGC ACATGTTGGG GCCAAAGTCT CTGCATCATA CCATCCAGTT CCTCTGAAGT 780 CACCGGTGCA GCAATCTCTG GGCTTCAGGG AGAAAAGCCG GCTCCGTGGG GCAATGAGGA 840 AGCAGGAGTA TGAGATAAAA TGTTTCCAGG GAGTTATCAG CTTTGATTGG AGGCTGGGAG 900 GATAATACTC AACGGAATGT CTCCAAGTCA CCCTCTCTGC CAATGACCTT CAGAAATCCT 960 TTCTCCAGGA GACAGGGGGC CATAATTCAG TAGCCTGGGG CCACAGGCTT CTGTTACTGC 1020 ACACTGCGTT TTAGGGGATG AGACCATATG AGGGGACTCT CTTGTCCCTC TCATCCTGCT 1080 GGGAAGGGCA TGCACCTCAC CTCAGCTTCA GCACAGGCTG CTTGCTGCAT GACTTCCCAG 1140 ATGCCTACTG GCCCTCCGAG CCCCAGTTCA CTCCTATCCC CTCCCCACAT CCCCTGGGCA 1200 GCAGATAAGA AGGGAAGGAG TCAGTGTAGT ATAGAGGAGA GAGCACAGAA CCAGGACTCA 1260 GGAGGGGCTG CAGCAGCCTC AGGCTGCTGC AATAACTTGG CCAATGTTCT GTTCCTCTCC 1320 TCTACAAAAG AAGAGCTTTG ACTGCATGTT CTCCGTGTTT CTTCTCTTTC TAACGTTTTT 1380 TTGGTTCTAA ATTACCCAGG ACTTCTAAGG AACCATGCAC TCTGGTGGGT GTGAGCAGAA 1440 TAATAGGGAG CTGAGAGGGA GCCCCTATGT TCTGGACTCT AGAACCCTTA CCTGGCCTCC 1500 TGGGAAGGAG CCCACCTGCT CTGGGAAGGG CACTGAGGAG CATGTGTGAC AGCTATGGCT 1560 GCAGTTCACC CCCCACATTC AGAGGCAAGA TCCCAACCTC CAGGAGAAAG CATCATTTCA 1620
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