Tag | Content |
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EnhancerAtlas ID | HS141-17424 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr7:102538360-102539400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr7:102539355-102539366 | AATTTAATTAA | + | 6.32 | Lhx3 | MA0135.1 | chr7:102539359-102539372 | TAATTAATTATTT | + | 6.71 | Lhx3 | MA0135.1 | chr7:102539356-102539369 | ATTTAATTAATTA | - | 6 | PHOX2A | MA0713.1 | chr7:102539354-102539365 | TAATTTAATTA | + | 6.62 | POU4F2 | MA0683.1 | chr7:102539358-102539374 | TTAATTAATTATTTAT | - | 6.65 | PROP1 | MA0715.1 | chr7:102539354-102539365 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr7:102539354-102539365 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr7:102539354-102539365 | TAATTTAATTA | + | 6.62 | ZBTB18 | MA0698.1 | chr7:102539314-102539327 | GCACATCTGGAAG | - | 6.17 |
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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 |
GH07I102898 | chr7 | 102539047 | 102539248 |
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Enhancer Sequence | CACTCCAAGT TTGAATGCTG TTCTCCCACT CCTTTTGTAA TATACTTATA ACATTGCTAT 60 AAAAATTAAT TACATGGGTA AAAATAGGGA GTAAGTATGG GGCGCCACAG CATCAGCTTT 120 CCTGCAGAAA CCACATCTCT AAGTTTTCTA AATCATAAAA GTGTCATTAG GATTGGCACA 180 ACCAATTTGT AAAACTAACA ATATCAACTA AAGCCAAACA AACACACCTG ACAACCCAGC 240 CACTCGACTC CTATACACAC ACACACATAC ATATATATGT GTATATATAC ACCCATGTAT 300 ATATTGTGTG TATACATATA TATCCATGTA TATATAAATA CACAAACATA TATATATCAA 360 ACAAAAATGT CTGCTGTGTT CACCAAAAGC AACGTACATG AATGTTCATA GAACTTTGTA 420 TACTTTTCTT TTCTTCTCTC TTTTTGAGAC AGGATCTCAT TCTGTCACCC AGGCTGCAGT 480 GCAGTGGCGC AATCATGGCT CACCGCAGCC TCAGACTACA GGCATGTGCC ACCATGCCCA 540 GCTAACTTTT TTTATTATTT GTAGAGACAG GGTCTCCCCT ATGTTGCTCA GGCTGGTCTT 600 GGACTCCTGG GTCTCAATCC TCCCACCTCA GTCTCCCGAA GTGTGGGGAT TACAAGCATG 660 AGCCACCGTG CCTGGCCACT TTTCTGTATT ATATTTTGGC CAAACTTACC CCAAAAAAGT 720 CATTAGGGAA GTTTCTTTGT TCACTAGGTC CCAACTGTCA GTGCCAGCAA AGTGGGAAGT 780 AGATTTCATC TGGCATCCTG GATGTTAAGG ATTGCTCTGC GGTCAATCAC AAGCATGTTG 840 AAAGCAACAA ATTCAGATAC ATCGTCAAAC ATGAGCATGT GACTAATGGT GAGAAACCTT 900 CACAACTTTC TCTCTTGCAC TTCAGTGATT TTCTCGAGTA AGGCTCTCCC TAAAGCACAT 960 CTGGAAGTAT TCTTTTATTT TTATTTATTT AATTTAATTT AATTAATTAT TTATTTATTT 1020 TGAGACAGAG TCTCACTCTG 1040
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