| Tag | Content |
|---|
EnhancerAtlas ID | HS104-06747 | Organism | Homo sapiens | Tissue/cell | HUVEC | Coordinate | chr10:16856180-16857560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr10:16857060-16857081 | ATCCCCTTCTCTTTCTCCTCT | - | 6.03 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 16856559 | 16856721 | | chr10 | 16857056 | 16857212 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH10I016814 | chr10 | 16856800 | 16857199 |
| Enhancer Sequence | GTAATGCCAG CACTTTAGGA GGCCAAGATG GGGGCACTCC TTGAGCCCAG GAGTTTGAGG 60
CCAGCCTGGG CAGCATAGCA AGACCCCATC TCTACAAAGA AATAAAAAAT AAAACCATTA 120
GCCAGGCGTG GTGGCGTGTA CCTATAGTCC CAGCTACTCG GGAGGCTGAG GTGGGAGGAT 180
TGCTTGAGCC TGGGAGGGTG AGGCCCCAGG GAGCTGTGAC TGCACCACTG CATTCCAGCC 240
TGGGTGACAG AGCGAGACCC TGTTTTCAGG AAAAAAAAAA AAAAAAAGAA AAAAAAATTC 300
TTACACTTAT AATTAATGTA GCCATGTGAA GTATTTTAAT ACTTGTATAT ATTAAGCACT 360
GTGTCAGTGT GTGTGCACTG CTGAGAAGTG AGCCCTGGTG GAGGCTTCGA AGAGCATCCT 420
GGAACCCCCT AGGCTCCGAG AAGTCCTGAG GTCAGGGAGT TTGCAGAGAG CAGCCTTGGC 480
TCAATGCTAC AGAAGCCAGA GGAGATGGAA TCTGCAAATC TCCAAATTCA CTTCCACCCA 540
ACTTCCCAAA AAGTACTATT ATCCGTTGTT AGCTACTTCT TTAGGAAAAT TTAAGAATGA 600
TCTCGCTTTT CACCACCCAA TGTTATACCG GAAATATATT TCAGGAAGCA AGTGGCTTTT 660
CTTCCTTAAT AAAAGCCAAG GCTTCAAAGA GATAACGGAG CTGAACCGAA ATAGCTAAGC 720
CATTCTCCCC ATTTATAAAT ATTACATAAA GTCTCCTCTT CAAAAGCCGA AGGGTACAAA 780
GCTCCTCTGC TGAAAGCAGC CTCTCTTCTA CCTGGTGAGA ATGAGTGCTG TAGGGAGGAA 840
GGCCATGGGG CCAAGGTTCC CGCTATGCAT CATCTTCCCT ATCCCCTTCT CTTTCTCCTC 900
TGTATCAACA GTGCCCCCAA TAATGACCAT GGTCATGGCA GAGCCGGGCA GGCGCAGCAA 960
GGGGCAAACT CAGATATCCA ATTCCAGAGG CATCTGCTCA GTTGCTGACA GCAAGGACCC 1020
TTACGGAATG CAAGAGACCA ACACACACCA AGCCTGAGAG GCTAACTAGT ACACAACCTA 1080
AGTTTAATGG CACGTATTTT CATAAAGCCT ACGAAACGCA AATCTACGTT TCCTCCCTTT 1140
TCCTTCTGCC AAGACATATC AATAGCATCA ACTCCAACCT CTGTCCCAGG CAGGTTTTCG 1200
AACCGTGAAA ACCGTGAATT CACAGTAAAC CTGACTCTGC AGTTCTCTCC ATGCCTAAAT 1260
GGCTATCCAT CGCCTTTCAG GGTCTCCTGA ACATCTCCCT TCTTCTCTCT TGTCACATCC 1320
TGGAGTTGAT ATCCCAAACT CACAGGCCTA ATCCATCATT CTTTCATTTT CTTCATTCCT 1380
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