Tag | Content |
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EnhancerAtlas ID | HS180-01782 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:55280710-55282370 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr1:55281317-55281333 | CTTGGGCTTTGACCTC | - | 6.04 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23292 | chr1:55279490-55281327 | Colon_Crypt_1 | SE_23292 | chr1:55281337-55282201 | Colon_Crypt_1 | SE_25256 | chr1:55279098-55282436 | Colon_Crypt_3 | SE_27955 | chr1:55279062-55282271 | Fetal_Intestine | SE_28877 | chr1:55279158-55282320 | Fetal_Intestine_Large | SE_50686 | chr1:55279568-55281983 | Sigmoid_Colon | SE_52829 | chr1:55279406-55282194 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I054813 | chr1 | 55279253 | 55282156 |
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Enhancer Sequence | GGGTAAGTGG GTCTGGGGTG AGGGATACAT GGGAACTCTC TCCTGCCTCT ACAGCCAACA 60 CCAAAGCCTC TTTGTCCCCA GGTAACCGAT GCTTTGAGTG AGCCATATGC CTCCCCTTTC 120 TTTTCCCCAA GGGACCTGAG GTCCACTCCC ACTGTCTTAT TTTCCTAAGG CATTGGTTCT 180 CAAACTTGAA CTGGTATTAG CATCACCTGT AGGACTTGTT AAAACACAGA TGGCTGGGCC 240 CCATGCCAGA GCTTCTGATA CAGTAGGCCT GGGTTGGGAC ATGGGAATTT GCATTACCAA 300 CAAGTTCAGG TGATGGCGAT GATGCTATTC CAGGGACCAC ACTTTGAGAA CCAATTAGCT 360 AAGAAACATC ACACCGCAGC CATGCCATTC TCTTATTTTC CCAGAGAAAT GCTCCTTCCA 420 TCCTCTGTGT TTGTCTTGGG CCTCAGGGGC AGCTGGTGAA GCTGGTGCAT TTCCCGTCCC 480 TCACTGAGCA AGACCCCCTT CTGGCCCCTT CCCTTTCCCA CTCTCTTCCT TCTCTCCAGA 540 GGCAGCCATC CCCAAGTGTG CGATGTATCT TTAGTTAGTG TTCTTGTAAA CCAGCTAAAT 600 TCTTGGCCTT GGGCTTTGAC CTCATTCTGT TTCTTACTCC ACCCCTTTTC AGTTTGTAAT 660 GCACCTTTTA TTGGAGTCTA ATAATCATAG AGAAAGGCGC TGAGTCCTAA GTGCACAGCT 720 CCATGAATTG TCACATAATG GCCGTAACTA TCCCCCAGAG CATTTAACAG CTCTCATTTC 780 CAGCTCCCCA AGAGCCCCTG CCATTCCCAC CCCCACCCCA ATTTGATAGC CTGTTCTCCT 840 GACTTCCAGT AGCACAGGTC AGCCGCCTCA CCTCCTTACC TCCCCACATG GTGGCAAGGT 900 CCTCAGTGTG CCCAGACCCC AGTGACTGAT TCTTGTGAGG ACCAGCTGGT TGTCCCCGAA 960 TCCTTCCTTT TTTTACCTCT AGCCTGCACC CCCTGCAGGG GAGAAAGTCT TTACCTGAGA 1020 GTCCCCAAAT GAAATGTTTA GACCAGAGCC AGATGACCCT ACTGCTACCA CAGAGCCAGC 1080 CACTGTGAAG TGGGAAGGGC TGATGTGAGG TCCGGGTTCT GGTGGCTCAG CTGACCGCAC 1140 CCCACAGGGC GGGAGAGCCC CTCTGCTGGC ACCTCCAAAA CCTGGGTGCC TCATGAAACA 1200 GGCTTCTCCC TTGTGGGAGG CAACTTCTGT TTAGCATGGG ACCAGCTTCT GGGTCCTAAC 1260 ATCTCCCCAG CCCACCCCTC AGGACTGCTT CTCTGCAGAT GGCCGGGTTC TTGTCCTGCC 1320 TTTATTCTGC CCTTGCCGTG TTACCTTGGG CAAGTTGCAT CTCCTTTCTC AACCTCTCTG 1380 TTGGTGCCTC TAGGATCTGT GACCCCGATA TCTGGGTGGG ATGCTGTATT CCCTTCCTAG 1440 GGCTGCCACA AACTAGGTGG CTTAAAGCAA CAGAAATATT CTCTGACAGT TCTGGAGGCG 1500 AGAAGTCTGA AATCAAGGCG TCTGCAGGTC CGTGCTCCCT CTGAAACCTG TTGAGAAGAA 1560 TCTGTCCTTG CCTCTTTGTA GCTTCTGGTG GTGGCCAGCA ATCCTTGATG TTCCTTGGCT 1620 TGTAGTCGTC ACTCCAGCCT GTCTCCTGGC ATGGCTGTCT 1660
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