Tag | Content |
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EnhancerAtlas ID | HS060-18708 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:10885280-10886310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:10886176-10886188 | GTTTGTTTGTTT | + | 6.32 | ZNF263 | MA0528.1 | chr2:10885893-10885914 | CTCCTCCTTTCCTCCTCCCCC | - | 6.95 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 10885753 | 10885945 | chr2 | 10885437 | 10885800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I010745 | chr2 | 10885277 | 10886436 |
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Enhancer Sequence | TGCCTCAGCC TCCCGAGTAT CTGGATGCCT GCCACCACAC CCAGCTAATT TTTTTGTATT 60 TTTAGGAGAG ATGGGGTTTC ACCATGTTGG CCAGGCTCGT CTCAAACTCT TGACCTCAGG 120 TGATCCACCC ACCTCAACCT CCCAAAGTGC AGGGATTATA GGCATGAGCC ACTGTGCCCA 180 GCCTATTTGT TACCTTTTTA ACCGTTTTTT TTTTTCTTTA GACAGAGTCT CACTCTGTCG 240 CCCAGGCTGG AGTGCAGTGG CACCATCTCA ACTCACTGCA ACCTCCACCT CCCTGATTCA 300 AGTGATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGACTA CACACCCTGG TAATTTTTGT 360 ATTTTAAGTA GAGACGGGTT TTCACCATGT TGGCCAGGCT GGTCTCAAAT TCCTGATCTC 420 AAGTGATCCA CCTACCTCTG CCTCCTAAAG TGCTGGGTTT ACAGGCATGA GCCACCACGC 480 CCGGCCAACC ATTTTTAAGT GTACAGTTCA GTGGCGTTAA GTACGTTCAC ACTGCTGTTA 540 CAACCGTCAC CACCCTCCAC CCACAGGACT TTTTCCATTT TGAAGAACTG AAACTGTATT 600 CATTAAACAG TGACTCCTCC TTTCCTCCTC CCCCAGGCCC TGGCAACTAC CTTTCTACTT 660 TCTCTCTGTA TGAATTAGGC TATTTTACGT ACCTCCTATG AATGAAATCA TATAGTGTTT 720 GACCTTTTCT GCCTGGCTTA TTTTACTCAG CATGATGTCT TCAATGTCTT ACAGCATGTC 780 AGAATTCCCT TCCTTTTAAG GCTGACTAGT GCCGCATCGT ATGGACACAC CACATTCTAT 840 GTATCCACTC AGCTATTGAT GGATGCTTGG GTCGCTCCCA CCTTTTGGTT ATTTTTGTTT 900 GTTTGTTTTT GAGATGGAGT TTGTGACCTC CACCTCCTGG GTTTAAGCAA TTCTCCTGCC 960 TCAGCCTCCC GAGTAGCTGG AACTACAGGT GTGTGCCACC ACACCCGGCT AATTTTTGTA 1020 TTTTTAGTAG 1030
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