Tag | Content |
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EnhancerAtlas ID | HS048-20928 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:102843300-102845070 |
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) |
ZNF263 | MA0528.1 | chr2:102843713-102843734 | AGAGCAGGAAAGGGAGGGAAA | + | 6.65 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 102843334 | 102845009 | chr2 | 102844840 | 102845062 | chr2 | 102844003 | 102844653 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I102226 | chr2 | 102842670 | 102846324 |
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Enhancer Sequence | CTTTTTGACA GTGGGAATAA CTGAGTTGAA GTACAGGGAA GCATTCAGCG GGGCCTGGGC 60 CACAGGGCGG CCTCTATTGC TTGTCTGGAG GTCAAAACAA ATCCCCAACA CCACAGCTGT 120 GGGTTTTAGT CTGTGGGCCT ATGTCCTGCC AGTGCTGTTT GGCATAGAAA TGCCTCAGTG 180 TGATCCTGAC TCTCTGAGAG CCTGGCATTT CCCACCATGG TGCTTGTGAC TATGCTACTT 240 TTGTTTTGTT TTGTTTTGTT TTGTCTTAGA ACAGATACAA TCTATTAAGG CCTTGCAAAA 300 GTAATAAATC TGCTCTAAAG TCCCCTAATT AGATGAAAAA AGAAGCCTGG TGCAGCTGAT 360 CTGTGTGGAG ATGCACGACT TTATACCTTT TAAGTCCAGA GGCCTGAGTG ACAAGAGCAG 420 GAAAGGGAGG GAAACTGGTT GTCTGAGAAC GTTTTATGGG CCAGCTAAAA CATAAAAGAG 480 GTCACTGGCA TCAAGTGCTT GCTTTGCACA TAAAATACAC AGTACGGTTG TTGCCCACAT 540 GTTTGATAAA ACGTGGCTAT TCACTAACTT GGATTTTTTC CAAATTAAAT TTCTGAATTC 600 AGAATTAGCA ACCCTGAGCA ATGTAGAAAG CGATAAACTC CTTTTTAATG ACAAAAGTCA 660 TCTGAACCTT AAGTGTCCAG TGCAACCTGA AGTGCTGCTA GTACTGTGGA TAGTCCGACT 720 GGGCATGGGG AGGGGGTCTC TGGTTTTGGC TCTGGCATCT GCAGAGGCCG CCCCGTCTAA 780 GCACACCCAT GACTGCTCTC TCCTGCTTGC GTCTTTGAGA AGAAGACAGT TCAGTCCCCC 840 ACCACTGATT GTTTTCTGAC ACAGAGTTGA GTGGTTCAGT TGCTTTCTAC TTTTTGACTA 900 ACAGAAGCCT GCGTCACTTT ACGTATTCTT CCTGGAAGCT CAGGCCCCAT GGTGTGTCTC 960 TCTCACTGTC TCTCTCTCTC ACTGACTCTG TCAGTGACTC TCTCACTGAG TCATTGCGAC 1020 TCCCAGGAGC GTGACTATAG CTGTGACTTA TGGGTGTTGT GCAGTGTGTG GGGAAGCTGC 1080 TAGTGAGGTC GAGTTTAGCA GGAAGAGAAA ACAGGAATAG TGACTCACAC GGAGTAGTGG 1140 GGGCTGGGCA GATGAGAGAG TTAGGCAGCC CCGCCCTCTG CTGAGACTGG GACGCAGCCC 1200 AGATTCTGCA ACAGTGGGCA GAGGATTTGG CGATGGAGGC TAACAGGCAG CCAGGGGTCC 1260 TTTTTTTCTT TATTTTTATT TTGCTTAATT CAGAAAAGTA TGTGTGCATT TTGTGATGAA 1320 ATTCTCTACA GCTCTGTCTA CGAGAACTGC CCTGTAATAT CTCTGTGTGT TGGCTTTAAC 1380 AGTGAGCTAC TGATGAGATT CTGAGATTAG TCCCAGATCT TGTTTATGTC CTTGTTCCCC 1440 TTGAGGATAT TTTCTGAGTT AAATCAGGAA ATACCGATTA ATGGATGAAA ATGAGAAAGA 1500 GAGAAATAAT GTCCTTCGTA GGATAAGTCA TTTACCCTGA CTAGGTTAGC TAAGCTGTAT 1560 CACTCAATTA ATAATTAGGT GTGCATGACT CACCATTTTA GAAGGAGCCA TTGACAGCCC 1620 TAGCTGAAGT CAGCAAGTTC TGTATCTTCT CTAGCAAGCC ACTGGAGCTT TACAAATTCT 1680 CCTGGCAGGG GTGCATGTGT GTACGAGGAT GGAAGGGTCT GTGCACGGAT CTCCTAGAGA 1740 GATTTGAAAA TGCCTCGCCT TACTCCAGAT 1770
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