| Tag | Content |
|---|
EnhancerAtlas ID | HS176-07638 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr11:77233040-77234030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr11:77233780-77233793 | AAATTAATTATTC | + | 7.34 | | MEF2A | MA0052.3 | chr11:77233720-77233732 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr11:77233720-77233732 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr11:77233718-77233733 | GAACTAAAAATAGAA | + | 7.13 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I077522 | chr11 | 77233341 | 77233430 |
|
Enhancer Sequence | TCTAGTCCTC ATTTTCATTA AAAACAAATT ATGATAGGAT TGCATTGTTT GCAAAATAGA 60
CTTTAGTCTT ATACTTGGTC AGATTATTTG CATAAAGTGC AGCAAGAATA ATTATTTCTA 120
CATAGACCTT TTAGATTGGC TTTAATGGAA CTCTGTTCCA CAAGGAATCT CAGATAAGAC 180
CTTTTAAAGC CAGGCCAGCG ATGGGTTTGT ATCCTCAAAT ACCTGCAAGT TGAATAAACT 240
TCTCTTTTCT TGAGGTCCCA AGAACATGTG GTTCCTGGGC CTGCTGGAAA GTAACATTCT 300
TTACTCACCA CAGGTTAGGA ATCCTGCATG GGGACTGTGT AGACAAGGGT GTGAGATCAG 360
GTTTCCCAAG GAGCTTTTCT TAGTTCTGCA AGTTGAGCTT GACTCCTTAA AGGGAAGCAC 420
ATACCCTTCC AGTCAAAGCC TTAGTAAGAC AACCAGTTTC TCCAATTGCA TCCTGTTGTG 480
AACATCACTA ATCATTGGAG AAATGCAGAT CAAAACCACA ATGAGATACC ATCTCACACC 540
AGTCAGAATG GCTATTACCA AAAAGTCAAA AAATAAAAGA TGTTGAGGCT GCAGAGAAAA 600
GGAAATGCTT ATACACTGTG TTAGTGGGAA TGTAAATTTA TTCAGCCACT GTGGAAAACA 660
ATTTGGAGAT TTCTCAAAGA ACTAAAAATA GAACTCTCAT TTGACCCAGA AATCCTATCA 720
CTGGACATAT ATCCAAAGGA AAATTAATTA TTCTACCAAA AAAACACATG CACTCATATG 780
TTCATCATAG CACTGTCCAC AATAGCAAAG ACATGAAATC AACCTAGGTG CCCATCAATG 840
GTGGATTAGA TAAAGAAAAT GCCATACATA TACACTATGG AATATGACAC AGCCATAAAA 900
AATTACAAAA TCATGTTCTC TGCAGCAGCA CACATGGAGC TGGAGGCCAT TATCCTAAGC 960
CAATTAATGC AGAATGGAAA GTCAAACACC 990
|
