Tag | Content |
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EnhancerAtlas ID | HS048-37367 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:91049770-91051680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr9:91051636-91051647 | GTAATTAATAT | - | 6.02 | HNF1A | MA0046.2 | chr9:91050920-91050935 | AGTTAATAATTTACC | + | 6.5 | HNF1A | MA0046.2 | chr9:91050920-91050935 | AGTTAATAATTTACC | - | 6.61 | HNF1B | MA0153.2 | chr9:91050921-91050934 | GTTAATAATTTAC | + | 6.23 | HNF1B | MA0153.2 | chr9:91050921-91050934 | GTTAATAATTTAC | - | 6.5 | NEUROG2 | MA0669.1 | chr9:91050441-91050451 | GACATATGTT | - | 6.02 |
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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 |
GH09I088434 | chr9 | 91049852 | 91051680 |
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Enhancer Sequence | AGCCTGGCCA ACATAGCGAA ACCTCACATC TACTGAAAAT GCAAAAATTA GCTGGGCATG 60 GTGGTGGGTG CCTGTAATCC CCACTACTTG GGAGGCTGAG GCGGGAGAAT TATCTGAACC 120 CGGGAGGCGG AGGTTGCAGT GAGCCAAGAT CGCACCACTG CACCCCAGCC TGGCTGAAAG 180 TGTGAGACTC CAGCTCAAAA AAAAAAAAAA AGCTTATCTT TGTCAGTATG TCTTGCTGTT 240 GTGTCATTGG ATAAATTTCT GGAAATAGAA TTGAGTCAGA TCTTCAATTC ATGTATGATT 300 TTGTGAGATC TCACCAGATT GCCCTCCATC GACTCTGTAT TATTTTGCAT TCTTTTTTTT 360 TTTCTTTTTT CTTTTTTGGA GATGGGATCT CACTCCGTCA CCCAGGCTGG AGAGCAGTGG 420 CACGATCATG GTTCACTGCA GCCTCGACCT CCTGGACTCA AGCGAATCTC CTACCTCAGC 480 CTCTAAGTCG CTGGGACTAC AGGCATGCAC CACCACACCC GGCTAATTTT TGAATTTTTT 540 AGGGTTTTAC CATGTTGACC AGGCTGTTCT TGAACTCCTG AGCCTTGTGG GCCATGGTGC 600 CAGCCCCATT TTGCATTCTT ACCAGCAATA AAATATGTAA AGAGTTTCTC TCTTCTCACA 660 GTCTTGCCAG TGACATATGT TGTCAAATAT GTGGTTTTGT CTGTCTTGTG GGTGAGAAAT 720 GGTGTTTCTG TGCAGTTTTA TTTGTGATCT TGGCTTGTAA GGGCCTACTT GGCCTTCCTT 780 TTTCTGATAT TACATCTATT TTTCTTTATT ACTTGCATAA GGTTTTTTTA CATCAGAGTT 840 ATTAACCTTT AATCTGTGAT AGGGGTCATT TACCTTCTTA CACTTCTGTT GTGTGGAGTC 900 AGTTTCTTGG AAACAGCCTT TCTTGAGTCC CTGGTCTCTC ACTCCCACCT GTATGGGTCT 960 GTCAGCCTAT ATCACATAAG TCTTGCTTTG GAACCTTCTG CTCTTCTAGG TTATATCTAT 1020 GGTTTCTCAG ATCCTATGTG TTTATGTTGC TTTTCTTATT TCCTGAAGGG TATCCTTCAG 1080 TAACTTCCAA AGAAGATGTG TATGAAATAT AAATTTTAGC CCATATATGT GTGGAAATGT 1140 ATATACTGTC AGTTAATAAT TTACCCAGGT ACGAAGTTCA GAGTTCAAAA TCATTTTGCT 1200 TCAATATTGA CAATATTACT CTCTTGTCTT ACTGTTTTCT AGCCCAGTTT TGTTTGTTTT 1260 AAAGAGGTGG GGTCTAACTG TGTTGCCCAG GCTGGACTTC AGTTCCTTGG TTCAAGTGAT 1320 CCTCCTGCCT CAGCCACCCG AGTAGCTGGG ACTACAGGTG TGCTCCACAG CGCCTGACTT 1380 TCTAGCTCAG TGTTGATGAC AGAAGAATAA TTTTAGACTA ACAGTTTTTA AACTTTACAA 1440 TCTTTCTACA GTTTTAGAGT TGCAAAGAGA TAACGGGCTC TATTTTTTTA GAGCAGTTTT 1500 AGGTACTCAG GAAAATGGAG TGGAAAATAA CAGAGTTCCC ATATATTCCT TTCCCTCACA 1560 AATGTGCAGC ACACCCTGCC CCATTCCTGT CCCAGCATCT CACAGTGTGG TACATTTGCT 1620 GGAAGTTGAT GAACCTTCTT TGACATGTCA TTATCACCCA AAGTCCATAG TTTACATTAA 1680 GGTTCATTCT TGATGTTTCA CTACCCTGAA AATCCCTTGT TTTCCCATTG TTCTTCTCTC 1740 TCTCACCCTT AACCCCTGGC AAGTGCTGAT TTTTTATTGT CTCCCTAGTT TTGTCTTTTC 1800 CAGAATAACG TCATAAAGTC GGAATCATAC AGCGTGGAGT CTTTTCAGAT TGGATTCGTT 1860 CACTTAGTAA TTAATATGCA CATAAATTTC CTCTGTGTCT TTTTTTTTTT 1910
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