| Tag | Content |
|---|
EnhancerAtlas ID | HS150-07006 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr21:38286040-38287530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr21:38286491-38286504 | GCACATCTGGCTG | - | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 38286965 | 38287194 | | chr21 | 38286729 | 38287179 |
| Enhancer Sequence | GGGCAACAAA GACTCCATCT TAAAAAAAAA GAAACTTGAA TGTGAACCTT GAAGCTACCA 60
CCCACTAGCT GTGCCTACTT AGACAAGGCT GTGAGAGGAC ACTTTCACAA AGAAATAAAG 120
GTTTTATCAT GTAAGTGAGC TACTGCTGAC CTCACCCCTA TCTGGTTTCT GCAGGAAAGA 180
GGTGTCATAT TCACAAGGGT TCTGTAATGG AAGGACTGTG GGCAGAGGTA AGAGAACCCA 240
AGAACAAGGA AGGGGTGCCA AAGCACTTGG AACCAGCAAG GGACTGAAGG AGCAAGAGGG 300
GGAGCTGCTA ATGGGAAATA ATATTAATAC CTTGACCTCT CTCAAATCCT GCCCATCAAT 360
CTCCTGCCAG TGCAGCCAGT GATGAGAAAC ATCCAGAGTT AGGAGCACGG GAGCCCAGGG 420
ATGGGCCGAC AGGTGAACGG TCCAGGGGCC AGCACATCTG GCTGGGTGGG CTTGCTGGTT 480
ATGCGTCCCC TCTCACATCC AGCCCTGCAC AACTCTGACT TAGTCCCAGC AACAACATGA 540
ACTTCTACAC AGCCTGATCT AGCGATGAGC CCAAATCGAT TCAGCAACTC CAAAGGACTT 600
AGGATTGATG TCATTGGCTA TCTAACCCCC AGGAATATGA GTTCCTCCAG GGCTGAACTT 660
GCCACAGGGC TTTCTAGATC CCCAATGCCT GGGACACAGT AGGCACTCAA TAAATGTCTG 720
TTAAGCGGTC TTCCTTTTAT AATGTAAAGT GATAGCTCAG GCTCAGACGC TGAAAGGCCC 780
AGGATTTACT GCATTTTTTT GTTACCTGCC AACTAGCGAA GACCACAAAA GGCTTGAGTA 840
GAACAGTAAA AGCAGGGAGT GAATAAGTCA TTTCTAATAA GGCTGGTTTT ATAGGCATCA 900
CACCTCCACC AAGCCAAACA GGCTCACTGT AGAAGCGGAA TCTATTCTGC AAGTGCAGAG 960
ACCAAAGAGA AAGCCAGGGT TGGCTCTAAC GGCGAGGGCG GCTCTATGGG GCAGCTCAGC 1020
CACTGCCTCC ACAATGAGAG ACGCGAACTT CCACTCACTG GTCTCGTGGG TGCGGGACCG 1080
ACACCCACAG GAGTCTCTGG GGCCTTCATT AAGCCTGCCC AAGGAAAACG CCCGCCATTT 1140
GTCTCAGCCC AACACAAACA GGCTTCTGAC AGAGCAGGCA GCGTGGGGGT GGAGGGCATG 1200
GAAAACGCTG GGGCTGAGCC CTGGGGGCCC ATAGGCAGCC CTGCCTGGTG CACCCAGAGG 1260
TGCCCATCCT AGCCGACATG CACACCAACG TGACCATTCA CACGTTCCCT TCCTTCTGAT 1320
GCTGACATGT CCCCCCGCCC CACCATCCTC AGCTATTTGC CTGTTACCTG CCAGCCCCAC 1380
CTGGGCTTCT TGTGGGGGCA GGGGACTCTG GCATGGGATC CTGCCCTCAG CTCTGCCACC 1440
ATCAGCTGTG AGGCCGCAAG AGGCACTCCC TGGGCTGACC GCAGCTTCTT 1490
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