Tag | Content |
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EnhancerAtlas ID | HS034-17641 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:187190460-187191310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr2:187190538-187190549 | AGGCCATAAAA | + | 6.02 | CDX2 | MA0465.1 | chr2:187190912-187190923 | AAGCCATAAAA | + | 6.62 | Foxd3 | MA0041.1 | chr2:187190619-187190631 | AAACAAACATTC | - | 7.22 | ZNF263 | MA0528.1 | chr2:187190833-187190854 | TTCTCCTGCCCTCCTTTCTCC | - | 6.11 | ZNF263 | MA0528.1 | chr2:187190848-187190869 | TTCTCCTGCTCCTCTTTCTCC | - | 6.45 | ZNF263 | MA0528.1 | chr2:187190842-187190863 | CCTCCTTTCTCCTGCTCCTCT | - | 6.79 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I186325 | chr2 | 187190366 | 187191630 |
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Enhancer Sequence | CGGCACTTTG GCATTTGAGA AAACAGTGGG AGCAGGAAGA TCACTCTCAC CTTCCCCTCA 60 TACTTTGTCC CTTGAAACAG GCCATAAAAT CTAACTGACA GTCCCCTGAA GAAGGTTATA 120 AGACCTTCAT GTGAAGGATG CCCACCCTAA ACCTAGAAGA AACAAACATT CTTAACTCTG 180 AAGACACAGG GACACAGAGA ACAATCTGAA CAAACAGGCC TTGCCAAAGT TCCCTGTAGT 240 TCATTCTCTT TAGATCATAT CCCATGTATC CAGTGTCAGG CTTCAGAACA TAATACTTCA 300 AGTATAGTGC CTTGGCATGC TGAGTATGCT GAGCTGAAGA AAACCAAAAG GGCCTCAGAA 360 GAAACATCTG ACTTTCTCCT GCCCTCCTTT CTCCTGCTCC TCTTTCTCCC TGAAGAAATG 420 CCGTAAAAAC TAGAATTCCT CTTCCCCAAA GCAAGCCATA AAACCTAGAA ATGTTACCTT 480 AACTTTCCCT CACCTTTTTG TCTAACAGTT GGCCATAAAG AAATGTTCTG ACATACCTTA 540 CCTGATAGAT CATAACACCT CATTCCTGAA GGGGTCCTGC CTAACCCAGG AAGAAGGAAT 600 GTTCCAGAGA GAAACCAAGA AGAATCTGAA CAGACAGGTC TTGCTAGCTT CCCACCTCTC 660 AGTCTATTAC CATTTGTCCA ATCACATTTC TACATGATTG TTCATTCTTC ATCAAATCTA 720 AACGTAAATT TAGGGCCTGT TTCTTTGGCT CTAAATTTCT GGAGGCTAAT TTGTCATTTA 780 AATTTTTGAT TAAATAAATT TGCATGTTTT CTCCTATTAA TCTATCTTCT TCTCAGGTTT 840 ATTGCAGACC 850
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