| Tag | Content |
|---|
EnhancerAtlas ID | HS106-02429 | Organism | Homo sapiens | Tissue/cell | iPSC | Coordinate | chrX:102996660-102998240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chrX:102997046-102997057 | AGGCCATAAAA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 102996679 | 102997400 | | chrX | 102997400 | 102997522 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI103740 | chrX | 102995500 | 102998222 |
| Enhancer Sequence | TTTTCCTGGC CCCTTACCCA ATCTTATTGG TGCTCACAAC ATCTTGGGTT TTTAAAAAAC 60
TCTATTGTGT CTCACATTCA TGTGTGTGAT TCTTCAGAGA TGCTCCTCCT TAGTAGCTTC 120
TAAGCTCCAC GAGGGTGAGG CCTGGGCCTG ATTTTCTCAT TGCTGTGCAC CCTACAGCAC 180
CTAGCTTAGG GCCAGGCACA GGGTAGGTGC CAGCTAAACA TTTGTAAATG AATACATGAA 240
TGAATAAATA CAAGAATGGA TGAGGAGGCA CTGGTGCCTG CCCTAGCTTG GACAACAGTG 300
CTGAGTGTCA GTTGCTCCAT GGGGGCTCAT CTTAGCTGCT CTGGTGGCAA GGTTTCTTGC 360
AGCATCATTG TCTTAGTCAG CTAGGGAGGC CATAAAAAAA TACCACTGAC TGGGTGACTA 420
AAAAATAAGC GAAATTTAGT TCTCACAGTT CTGGAGGTTG GAAATCCAAG ACCAGGGTGC 480
CAAGATGGTC AGGATCTGCT GAGGGCCCTC TTTCTAGTGA AGGAAATCAA AATATTTTAC 540
CCCAAAATAT AATTTTTTGA CATATTTTGA AATGACTGCT CAGAGGGCCT GCAAACTCAA 600
GTAGCCTTGC AAAGCTGTCT TCTGTAGGGG AGATTTGCAT TTGTAGAGAA AACCTGCATC 660
GCTGCAGCCA GACTTTCCAA AGGCCTTTCC TTTTTGGGAT CTAGGAACGA TTAACTGAGA 720
TTCTGACAAC TTTAAAGGTC TGAAAGGAAC ATTTACCACC TATTCTCTGT GAGAGCTGCT 780
ACTTGTGAGG TTTCATTTAC ATAACAAGAC TGCATTTGCT GGCCAGGCCT CCTCTTCTTT 840
CTCTCATTAA CCTGTTTTGC CACTCCAGGC CCCCATTCTT TCTGTAAGAG AGAGAGAGCG 900
CGTGCACCCT AGTCTCTTCC TCTTACTTTT ATTTTATTAT TTTTTTGAGA TAGTGTCTCA 960
TTCTGTCGCC CAGGCTGGAG TGCCGTGGTG TGATCACAGC TCACTGCAGT CTCAACCTTC 1020
CTGGCTCAAG CGATCCTCCC ACCTCAGCCT CCCGAGTAGC TGAGACTACA GGCACTTGCC 1080
ACCACACCCG GCTAATTAAA TTTTTTGTTT TGTTTTCTTT TAGGGCTGGG GTGTCACTAT 1140
GTTGCCCAGG CTGCTCTAGA ACTCCTGGGC TCAAGTGATC CTCCTGCCTC TGCCTTCCAA 1200
AGTGTTGGGA TTACAGGCAT GAACCACCAT GGCTAGTTTA AATGGTTTTT CAGGGTCACA 1260
TATCTCGGAA GATATGTGGG ATGTAAACCC AGCAGCCTGG CCCCAGAGCC CATGGTCTTC 1320
ATGGCAGCAG CATGTGTGCC GCCTCTCATG TGTACAAGTG AATGAAGAAT GAAAGGTAAG 1380
CAGCGCACCG TGGTCATCCC CGCAGCCAGG AGCCTCCAGA GGTGCCATTC AGTCTCTCAA 1440
GTCCCTGGGT TTTGGGGACT CCCTGTCACA ACCCCTTTGG GGTAGCCTCC CACCCCTGCC 1500
ACTGCATCTC TTCCTCCCCT TGTCTTCTCT CTGTCTAATT GTGAGTGCTG CGCTAAGTAG 1560
GTCACTCCCA CTGAGGGCTT 1580
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