Tag | Content |
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EnhancerAtlas ID | HS060-23666 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr22:50204140-50205580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr22:50204889-50204910 | GGAGGATGAGAAGGTGGGAAG | + | 6.67 | ZNF263 | MA0528.1 | chr22:50204886-50204907 | GGGGGAGGATGAGAAGGTGGG | + | 7.05 |
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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 |
GH22I049811 | chr22 | 50205281 | 50205430 |
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Enhancer Sequence | CTTGTAAATG TTTGTGCTTC AAAGAACACT GAATAAAACA ATAAGATGAC CCACAGAATG 60 AAGAGAAAGT ATTTGCAAGT CATGTATCTA ATAGGGAGTC TAGTACCCAG AACAGAGAAC 120 TCTTATGACA ACAGTAAGAA GTCAGCTAAC CAATGAAAAC ATGGCAAAGA TCTGAACAGA 180 CATTTCTCCA AAGAAAATAT GCAAATGGCC AGGCAACATC TTCAGCCACT GTGGAACTGC 240 AAAGCAAAAC CCCCGAGCGA TCGCTGCCCC TGCACCATGG AATGGGTATC ATCAAAAGGA 300 CAGCGCCTGA GAATATACAG GGGTACAGCT GCCTTGGAAA ACAATCTGGC ACTTCCTCAA 360 AATACTAAAC AGCATTACCA CATGACCCAG CAACTCCACT CCTAGAATAT ACCCAAGAGA 420 AATAAAAACA CACTACCTAA AAACTGTTAC ACAAATGTTC AGAGCAGCAT TGTTCATAAT 480 AGCTCCAAAG TAGGAAAAAA ACAAACATCC ATCAAAAGAT GAACAGATTT TTTTAAACGT 540 GGCCTATCCA TACAATGAAC ATTACGCAGC CGTGAAAAGG AATGGCACAC CGACCCAGGG 600 GGCACGATGG ATGGACCTTG GAAACATGCT CAGTGAAAGA ACAAAAAAAA CACATTTCAT 660 AAAAGAACAA AAAAACACAT TTCTATGAAA TGCCCACAAC AGGCAAATAC ACGGAGACAG 720 GATGCAGATG GGTGGCTGCC AGGGCTGGGG GAGGATGAGA AGGTGGGAAG TTGGGGTAAT 780 GGCTAAGAGG CACAGGGTTT CCTTTGGAGG TGATAAAAAT TTCTAAAATT GGTGGTGGTG 840 ATAAATGCAC AACTCTGTGA ACTAAAATCC ACTCAACTGT ACACTTCACA TGGGTAAATT 900 TCATGGTGTG TGAATGACAA GAGTCCCCCC TTAACCAAGG GGGATGGTTC CAAGACCTCC 960 AGCGGCTGCC TGAAACTTGG AACAGGACCG AGCGCCAGCC TGGATGTTGG TACCTGCTAC 1020 TAAGCGGGTT AAGGTGCAGG CAGCTGCACG GCGTGGGTGC ACTGGACAAA GGTTAGATTC 1080 ACGCTCCCGG CAGGCAGGAC ACGACAGGGA GACTGTGATC ACGCTGCTCA GAATGGTGCA 1140 CAACTGAAAA CTTATGAACT GCTTACTGCT GGAATTTCCC ATTTAATACT TTCAGACTAT 1200 GGCTGACCAT GGGCAACTGA CACCATGGAA AGCAAAACCA CAGGTAAGGG GAGGGTACTA 1260 AGTGTCTCAG TGAAGCTGAC AAAATTCCCC CACGGGCGGC AGAACAGGGA TGGAATGGGA 1320 CACACCGCAC AGGCGAATTC AGCCGGCGGT GCTGAGTCTC CCAATTCCTA GGCTATGGGT 1380 GGGTTTGTGG GCATTGCTAT TTACATTTAT GGTCCACACA TGATTTGGCA TGTATCAAAC 1440
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