Tag | Content |
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EnhancerAtlas ID | HS180-09281 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:73622730-73624150 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:73623555-73623576 | CCCTCTCCCTCCCCCTCTCTC | - | 6.19 | ZNF263 | MA0528.1 | chr11:73623549-73623570 | ATTTCTCCCTCTCCCTCCCCC | - | 6.49 | ZNF263 | MA0528.1 | chr11:73623564-73623585 | TCCCCCTCTCTCCCTTCCTCC | - | 7.87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I073911 | chr11 | 73622180 | 73623897 |
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Enhancer Sequence | CGATCTCTTG GCTCACTGCA GCCTCCACCT CCCAGGTTCA AGTGTTCGAG TGATTCTTGT 60 GCCTCAGCCT CCCGAGTAGC TGGGATTACG GGTGCCCACC ACCATGCCTG GCTAATTTTT 120 GTATTTGTAG TACAGATGAG GTTTCACCAT GTTGGCCAGG CTGGTCATGA ACTTCTGGCC 180 TCAAGTGATC CACCCTCCTA AGCCTCCCAA AGTGCTGGGC TTACAGGTGT GAGCTATGGG 240 CCCCAGCCAC CAGTGACCTT CTTCTTGCCT AATCCACCTT GTTTCTCTGT GCTTGTCTTT 300 CTGAATTCAG TGGTATTTCA CATAGTAAAC CCTCTCCTCA AAAAACTTTT TTTTTTCATG 360 GCTTCTGTGA TACCACATAA CACTGGTTTT CTTCCTATTT CATTGACTGC TACTTCTTAA 420 AGGTCTCCTT TTATGAAACT CCTCTCTTCT ACCTTTAAAT ACTAGAGGGC CCCACTATTA 480 AGTTCTGGGC CCTCAGCTAT AACTACAGTT TCTTCCTTTG TGACCTCATC TGTTCTATAG 540 CTATCATTCC AAAGTTCATG TAAAGCATAG ACCTTTCACC TGAGTTTCAG ACTCTATTTC 600 GATGTCTAAT AAATAAGTTG AACTTACCTT GTCTAACAAG GAGTGTTTGA TCCCTCCCCA 660 CCCCAAACTG TTTTTTTCCA TCTCAGAAGA TGGCACCGCT ATCTACCCAT TTGCTCAAGC 720 CCAAAGCCTG AGATTCACTC ACAGTCCACC CTCTCTTTCC TCATGTCCCA CATCAGCAAA 780 GTCTATCATC TCTAACTTCA AAGTGTTTCT AATTTTTCTA TTTCTCCCTC TCCCTCCCCC 840 TCTCTCCCTT CCTCCTGTCA ACATCTGGTC CAAACTATCA TCATCTATTG CCTGTACTAC 900 TGCCTAGACT ATTCTCCTAT AAGCCATTCT TTTCAGAGCA ATCTTGTGGT CATTTAAGAA 960 AATCATAAGT CATGTCACAT TCCTGCTTAA AACTCTCCAG TGGCCTCCCT TTATAAATAT 1020 GTTGAAATCC TAACCCCTTA GCATGGTTTA CAACAAGCTC TTATACTTTC TGACCCCTAC 1080 ACTTCTCTCC AGTCTCATGT CATACCACCC TCTGCCATGT TCACTACATT TCAGCCACAG 1140 GCCTTCAGTT TCTTCTTTCA GTACAGTAGA CTCTCCCAGT CTCCTGGACT TTGCCTTCTT 1200 TTTTTTAAAT TGAGATGGAG TTTCCCTCTT TTGCCAGGCT GAATGCAGTG GCACGTTCTC 1260 GGCTCACTGC AACCTCCACC TCCTAGGTTC AAGCAATTCT CCCGCCTCAG CCTCCCGAGT 1320 AACTGGGATT ACAGGCGTGC ACTACCATGC CTGGCTATTT TTTGTATTTT TAGTAGAGAT 1380 GGGGTTTTGC CATGTTGGCC AGGCTGGTCT TAAACTCTTC 1420
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