Tag | Content |
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EnhancerAtlas ID | HS048-01217 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:45909270-45910720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr1:45909874-45909884 | GCCATATGGT | + | 6.02 | NR2F1 | MA0017.2 | chr1:45910636-45910649 | CAGAGGTCACAAG | + | 6 |
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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: 2 | ID | Chromosome | Start | End |
GH01I045443 | chr1 | 45908921 | 45910436 | GH01I045444 | chr1 | 45910641 | 45910790 |
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Enhancer Sequence | ATACAAATAA ACTACATAAA TCCACACTCT AATTGTAAAG TAATCCATCA ACCAATCTTT 60 ATTTTGCTAT CTAGGACAAC TAAAAGTCCT TAAGTTACCT GCACTAGAAG TCAAATATTT 120 CCTTTTATCA CCACTGATAT ACTTTTTATT TAACCTGACC TTTAAAGCTC GATAATCATC 180 TGTACTTTGT AATCAAAGAT AAAACTAAAC ATCACCTACC GGTGCACTAC AGCTATTAGA 240 TCAGGAGTCG GCAATTTTTT CTGTAAAGGG TAAAACAGTA AATATCTTAG GCTTTGAAGG 300 CCAGGTACAG TGGCTCATGC CCGTAATCTC AATGCTTTGA GAGGCCAAGG TGGGAGGATT 360 GCTTGAGGCA GGAGTTTGAC ACCAGCCTAG GCAACATAGC GATACACTAT CTCTACAAAA 420 AAATTTAAAA ATTAGCCGGG TGTGGTGGCA CATGCCTGCA GTCCTATCTA CTTGTGAAGC 480 TAAGATGGGA GGATCCCTTG AGCTCAGGAG TTCAAAGTTA CAGTGAGTTA TGATCATGCT 540 ACTGCACTCC AGCCTGTGTG ACAAAATGAG ACTCTATTAA AAAAAAAAAA AAAAGGCTTT 600 GAGGGCCATA TGGTCTCTGT TACAAAGTAC TCGATGAGTA CAGATGTGTT CCAATAAAAC 660 TTTATTTCTA AAACTTTGGT CCAAGGGCTG TAGTTTACCA AATACTGTAT CAGACTATAT 720 TATATGCAAC CAAAAATAAA CAGACCTATT CCCCCCTTTC CCATTGATAA TGTTTTCACC 780 ATAAAATTAA ACAATTACTT TCTAAAATAC CACAAAATAC ATTTAACTAG CTTTCTTCTA 840 TTTTGTAATA GGCATTCATA GTGGGATAAT GCTATCCCTA TTGCCTCAAA TGAGGAATAA 900 CAGCCAACTA TGAGATTCAG GTTTAGGATT CAGATTTGAA CCACACACAC TGTACAGAAA 960 GACTGAGCCA ATAAATAAAA ATAAAGCATT TAGGTTCACA TCCAGAATCT ATTTGACCCC 1020 AGCAGAGGCA AAAGTTAGTT CACCATATTG GAACATATCC ACAACCTAGA ATAAAATAAC 1080 TCCCAGGGAA AATGAAACCG CTTTTGCAAA ATTGTAACAG TAAGAGAAAT CTAACATCGC 1140 TGACTCCATC TTGCTTCTAA CCACATAAGC TAAACTGTCC CTGTCCATAT CCGGGCATAA 1200 GCCAAGCTAA CTATGGGAGG AATTTAGCTC ATGGTTTAAC TTTAAAACAA AGATGATAAC 1260 AGTCCCTTCA GGAAACTAAC CCCCTGCTTG CTTGGGGATG AAACTGCCTT TATAAAACTA 1320 ACAGACTGGC CACACAGTTA GAATTATGGT TCAGGGGTCA TGCAGCCAGA GGTCACAAGA 1380 TTTGTAACTT CCCCAATTGC TCCTACAGAT AACATCACTA TTGCAAAACC TAAGACTGGT 1440 GTTTGAGTAT 1450
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