| Tag | Content |
|---|
EnhancerAtlas ID | HS078-00234 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr1:10020070-10021760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF410 | MA0752.1 | chr1:10021563-10021580 | CCCCTCCCATAATACCA | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 10020769 | 10020829 | | chr1 | 10020862 | 10021545 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I009960 | chr1 | 10020686 | 10021970 |
| Enhancer Sequence | AGCCATGTTA CTTAACTCTT AGCCAACACA GGTTTAATAC TGAGCATCCT GAAATATGCG 60
ATAGGGAAAG CCAAACAGAA TTACTATTGT TTTCGAAAAG TTGATTTTTA AAAAACTGAC 120
TTTTTAGCCA GGAGTGATGG CGTGTGCTTG TAGTACTAGC TACTTGGCAG GCTGAGGTGG 180
GAGGATCTCT TGAGCCTGGG ATTTGAAGGC TGCAGTGAGC AATGATTGTG CCACTGTACT 240
GCAGCCTAGG CAACAGAGCG ATACCCTATC TCTAAAAAAA ACAAAAACAA AAACAAAAAA 300
ACCCTGGCTT AATGTTATGT TAATATTTAC ATCTCAGTGT TTTTAAAACA TAAAGATCAG 360
TTATTTTGGC CAGGTGTGGT GGCTCATGCC TCTAATCCCA GCACCGTGGG AGGCCAAGGT 420
GGGAGGATCA CTTGAGGCCA GGAGTTTGAC ACCAGCCTGG GCAACACAGC GAGACCCCAT 480
CTCTACCAAA AATAATAATA ATAATAAAGA TCAGTAACTA CCCAGGCCAA AACGCAGTGG 540
CTCAATTTCA GCCTCCCGAG TGGCTGGGAC TACAGCCACG TGCCACTGTA CCCAGCCCAA 600
GATTAGTAAT TTTAAAATTA AAAGTAAATT TTAAGCCTCA AGACTGCCAG AGAAAGAAAT 660
GAACTCCTTA TTGTCACAGT GAGCTGAGGA GGGACACTTA CAGCCTGAGC TGGTGAGTTC 720
TCAGCAGCCA GCAGTGCAAG CGATAGGCCG TGTGGGCCAA ACAAAAGTGA ATCATGGTGA 780
CACTGGGCCC AGAGCACCTG GAGCAAGACA AGGAGGACCC AGGTCAGTCC CGTTAGAGTT 840
TCCAAACTGC TGCACCCATT CATCAATCGG CCACAGCCCC CCTATACGCA TGCGCATGTG 900
CCCTGCAATG ATATGGAGGA AGTACTCTTC AGGAAAGGGA CAGACCCTAG TTCTTTAAAA 960
CCCACTTTTG GCAGCAATAG GAGCTCACTG TAACCTTAAC TCTTGTGTGG CTCTGAAGGT 1020
TTAGAGTCTG GTGTGAGCTC GAGTTGGCTT TGTTAACAGT TAGTGGAACT GTGAGCTGGA 1080
TATTTGAGAC AAGTTATAGA TGTAACAAGG GAGAAAGACA GCTTCCTTTA TGCTGAGAGA 1140
TCAGCTTCCT CCAGCCCTTC CACATCCCTT GGGCATCACC TGGAAACCTA AGCTTATCCC 1200
CAAGTGTAGG GCTAAAAGCT GTTTGTTCCA TCCTTCCCTG AAGTCTGCTT CAGAACTGCA 1260
GCAGCTCCCT TGAGGACCCA CACCTCTCGA ACTCAGCCTT ACCCTTCTTC CATCTCTCTC 1320
TTGGGAATAG TAACTGAAAC CTGAGATGGG CGGGGTTGTC TGACGCCAGC TGTCTGTCTG 1380
GTGCCAGCTG AACCCAGCCC CTCCACCAGT CTTTGAGAGC ATGCTCAGTG GCTGGTGGAT 1440
ACCCTGATTT CTCTGTAGGC CTCAGGGTAC TATGGGCATG TCGCATTCAT CACCCCCTCC 1500
CATAATACCA CTGGTAGTTT TTATGGGTAT CGAGGGCCTG GGGTAGGGAT AAAGGGTATG 1560
GGTACAAGCC CCAAGTGAAT CATGGTATGA TACTTTTGAT GGTAACTGAA AGGTAAGACA 1620
TTTAAATCAT TCTTAGTGAT GAACTCATTT TTTTCTAATG CCCTAGTGAC TACTACTGAA 1680
CCTTCTCCGT 1690
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