| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06211 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr11:86046070-86046740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr11:86046346-86046356 | GACATATGTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH11I086334 | chr11 | 86045929 | 86046533 | | GH11I086335 | chr11 | 86046561 | 86046710 |
| Enhancer Sequence | AGTAAGAACA GTGAGCTTTG TGGCATTTGG CTACCCTTGT CCCATCTGCT TCTCAGCTCA 60
GTGATAGCCT TGAAAATAAC AGACTCCATT CCTGGTACTG ATATAGGGAG CAGGATAGAC 120
CTAATTCAGA AAGAATTGTA ATTAACTTGT TTTCATCTGT CTGGTGGCTT GCTAGAAGAC 180
TGTTTAAAAA AAAAGAGGTC TGCCTTTATG TCACCTAACT TGGAACTCTT CATGGAAAAG 240
TATCTACCTT GGGGGTGTTT GTTAAAAGTA TTTACAGACA TATGTTTTAG CTACTGTTGC 300
CCGAGGCAAA GGAAAACAGT TGGAGTAAAC CAAAACTAAC CAGAAAGGTT GGGAATGAGA 360
TGCTTTGGGG AATGAGGGCT TTGAAATTCT CTGACATATT CTTGGTAATC TAGAAGGGTA 420
CGTGCATTCC CAGAGCTTTG TGCATGCTCA GGAAAGACCC GCGAAGACCC AGAGCTCTCT 480
CTTCTGGCTC ACTTTAAGTC TCCGCACAAG CAGGAAGTGA AGACTAAGGT GGAGTTATAA 540
ACTGCCTGGC TGAATACTAA AGGCATGTCC CAACACGCAG AGCCCATCTG CAAAGACTGG 600
CAGAATTTTT TGGTTGCAGA GGTTTAAGGA AATTTCTTTC TAATCACTAG CAGACTACTA 660
ACTAATGGAA 670
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