Tag | Content |
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EnhancerAtlas ID | HS048-21156 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:121044560-121046130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT2 | MA0756.1 | chr2:121046098-121046112 | TAAAAATCAATACA | + | 6.03 | ONECUT3 | MA0757.1 | chr2:121046098-121046112 | TAAAAATCAATACA | + | 6.33 |
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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 |
GH02I120286 | chr2 | 121044035 | 121046183 |
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Enhancer Sequence | TCCTACATAA TTGAGTTTTA AAAAATCTGT TCTTCTTATA AACATATCTA TCTAGATGAC 60 TTTTTAAGAA GCAGATCTAG AGTTTAGTAG GGAACTGAAG AGAAAAAACC CAAAAATCAA 120 ATCAGTTTTT TTCATTCTTC AGCAAGTTCT GGTCTGACAG TAAGGTGGTC AACCAGAGGT 180 GAAAAGGAGA AAGCTAGCTA TCCTTCCAGG ACTTGGATGG AAGCATCACT GAGCCAGGGA 240 GGCCTCGGGT GAGCACAGGT CACCCAGCAG GGCTAGTGAA AGATAATAGG GAGGTGCCTC 300 AGTGATGCTT CATAGCTCCA GGCTTCAGAG TCGAAGACCT ACTTTTCTGG AAGCAGAGTG 360 CGTGTGGTGC AGTGACTAGT TAAGTGACTA TGACTCATTA TGAGAAGTTC TGTTAATTTT 420 TAGACATTTC AGACCTTCCT AAGGGCTGCT CTGTTTGAAT GTAGCCCATG TATTTATAAT 480 TGTTTGCATC TGCGTAGTCC TGTTTTTAAT GCCTCATAGA GGGTAAAACA GGACAGATGC 540 ACACACTCTC TTCTTTTCTT CCCTGTCCCG AGCCTTTTGA TTTCCTGTTG TTCTGTGACT 600 TACTTAGAAG GGAAGTGGGC AGGAGAGTTC TCTGCAGAGG ATATGGAGAA ATACAGGTAT 660 TTCAAGTGCT CCTTGTCCTC TCCTCAGTCA CCACACATGC ACAGATAGCA CTCGGGCGTT 720 CTCACAGAGT TGGAGCAGGG CTCCCCTCAA TGTGGAAAAG GGTTTTGGTT GTTAGGTGGA 780 AAGAGAGATC CTTAGAAGAA AAAGGACAGA TGAATACCTA AAACCAGAAA GAAGGGGAAG 840 TTGACCTCTG CGTAGGTTTC TCATGTTGTT GGGAACAGAA GAATGCAGGT CAATTATCTG 900 AGCCCTGTGG CTAAACTCAA GTCACTTTAC TTCATGTCTG TTAGCAGTTT TAAAACAGCA 960 TTTGTGTACT ATCTTCCAAA TAGAAAGGCC CCAATATAAA ATGACATGTG AATATGCTGT 1020 CTTCCTTGAA ACTTTTTCTG GAAAATATTT TATGAACTAA GATAAGTTCT GTCATAAGAG 1080 ACCAGAACTT GGTACTCCCA TTTTTGGATC GATATGTTTA TCAATGAGGT AATTTTGTGT 1140 GCCCCTGCAA GACTAATGAG CCAGAAAGCT ATCAGTTTTT ATTGTTCATA GTTTATAATG 1200 ATCACATGAC TTCAAATGTA TCATGTTCTT TGACCCCAGT TCAAATGTAG GCTATAACAA 1260 GGCTACACAA AGCCAATTTC AAGCATCTTT TCATCTTTTT TAGTTTGTCT TAAAATATTT 1320 GATGTCTGGC ACTTAAATTG ACTACATGAA AATTTTAGTT TTTTTTTTTG TTTTTTTTTT 1380 TGTAGATACA AGGTCTCCCT ATGTTGCCCA GGCTGGTCTT GAACTCCTGG GCTCAAGTGT 1440 TCCTCCCTCC TCAGGCTCCC AGAGTGCTGG CATTACAGAT GTGAGCCACC ACGCCTAGAA 1500 AATATTTTTA TTATTGTGAA ATGTTACCCT ATACCATATA AAAATCAATA CAGATCTCTA 1560 CAAAATACAT 1570
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