Tag | Content |
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EnhancerAtlas ID | HS129-07299 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr11:86046020-86047120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG2 | MA0669.1 | chr11:86046346-86046356 | GACATATGTT | - | 6.02 |
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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: 2 | ID | Chromosome | Start | End |
GH11I086334 | chr11 | 86045929 | 86046533 | GH11I086335 | chr11 | 86046561 | 86046710 |
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Enhancer Sequence | AGCTTGTAGC AATCAGGGGA ACATTTAATC AAGAAAATAC ACTGAATCTC AGTAAGAACA 60 GTGAGCTTTG TGGCATTTGG CTACCCTTGT CCCATCTGCT TCTCAGCTCA GTGATAGCCT 120 TGAAAATAAC AGACTCCATT CCTGGTACTG ATATAGGGAG CAGGATAGAC CTAATTCAGA 180 AAGAATTGTA ATTAACTTGT TTTCATCTGT CTGGTGGCTT GCTAGAAGAC TGTTTAAAAA 240 AAAAGAGGTC TGCCTTTATG TCACCTAACT TGGAACTCTT CATGGAAAAG TATCTACCTT 300 GGGGGTGTTT GTTAAAAGTA TTTACAGACA TATGTTTTAG CTACTGTTGC CCGAGGCAAA 360 GGAAAACAGT TGGAGTAAAC CAAAACTAAC CAGAAAGGTT GGGAATGAGA TGCTTTGGGG 420 AATGAGGGCT TTGAAATTCT CTGACATATT CTTGGTAATC TAGAAGGGTA CGTGCATTCC 480 CAGAGCTTTG TGCATGCTCA GGAAAGACCC GCGAAGACCC AGAGCTCTCT CTTCTGGCTC 540 ACTTTAAGTC TCCGCACAAG CAGGAAGTGA AGACTAAGGT GGAGTTATAA ACTGCCTGGC 600 TGAATACTAA AGGCATGTCC CAACACGCAG AGCCCATCTG CAAAGACTGG CAGAATTTTT 660 TGGTTGCAGA GGTTTAAGGA AATTTCTTTC TAATCACTAG CAGACTACTA ACTAATGGAA 720 CAGAGACTTC ACTGGCCACA CATAACAAAG AAACAGACTT TACAAAATTA GTTCAGATAA 780 GTCATTAAAT GAGGAAACAA CTACAATAAA CAGCAACAAC AAACCCCTAG AAGGTGGAAA 840 CATCTGATTT ATAGCGTCGT CACATTGTAA TATTCAAAAT GTCCAGTTTT CTACAAAAAA 900 TTATGAAACA TACAAAGAAA CAAAGTAAGG CTCTTATACA GAGGAAACGA ACAGAAACTT 960 CCCCCAGGGA AGCACAGGCA AAGACTTTAA GTAAGCTGTC TTTATTATGC TCAAATTGCT 1020 AAAGGAAACC AGAAGAATGA TACATCATCA AATAGAGAAT ATCAATATAG AAATTATAGA 1080 AAGGAACTAA ACAGAGTTTA 1100
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