| Tag | Content |
|---|
EnhancerAtlas ID | HS175-12132 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr18:10213000-10214200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr18:10214144-10214155 | TTAATTAAATT | - | 6.32 | | Lhx3 | MA0135.1 | chr18:10214150-10214163 | AAATTAATTATTT | + | 6.78 | | MEF2C | MA0497.1 | chr18:10213259-10213274 | TTCTATTTTTATTTT | - | 6.21 | | PHOX2A | MA0713.1 | chr18:10214145-10214156 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr18:10214145-10214156 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr18:10214145-10214156 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr18:10214145-10214156 | TAATTAAATTA | - | 6.62 | | RREB1 | MA0073.1 | chr18:10213630-10213650 | CCACAAACCACACCCCTCAG | + | 6.07 |
|
| | 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 |
| GH18I010213 | chr18 | 10213311 | 10214121 |
|
Enhancer Sequence | GTGTGTGTAT ATATCTCTTC CTTTGGAAAA CATAAAACCA TTATTTTAAA GTTAATCTTA 60
TGACTTTTTA ATTATATATT CAACAAATTA AAGTTTACTA GCTTCCAGTT GTGTTCAAAT 120
TATTTATGCA GATCTTGATT AGTTAAACAA AATTTACCAG ACGGGGAACA TGATTCATAT 180
TTATAAAGGC AAAATGCAAC TAAATTATAG TAGTTTTTTA AATATCCAAC TCTTCAGAAC 240
CAAACTTTCA AAATCAGGTT TCTATTTTTA TTTTTCAATA AAAAGTTTTG AAGATTTTAA 300
CTGACCCATG ATTTTGAGAA TACTATGGAG TATTAACACA GATAAACTCA TTTCAATGGA 360
TACGAATTAA TCAAAGGTTT GTCTGGACTA TTTTCATGTC CTCCCAGGAA TTCTACAGTA 420
ATGGTAATTT TTTTGTTCCT TGCAATGAAT AATTCAACTT TCTCAGTTAC TATATCTTTA 480
ATAGTCATTC AGAAATAATT TAAGATTATG TGGCATTTGT CAAACAAAGG AAGACTGATA 540
AAACCAAGAA AGGTAGTGAT CTGAGTTAAT TATTTTTCTG TTTGCTCTAA AGAAAAGCAA 600
ACTCTTTAAA TTCTTACAGA TATCACTCAG CCACAAACCA CACCCCTCAG AAAACACACA 660
AGAAATCCAT AGCCACTTAA AAACACAAAA CCAACGTGAA GCAATCCTGA TGCTTAAGAG 720
GCAAAGCTGC TTGGTTCCAC TTCCTGTTTC TAACTGTTGT TGACAGAGTA CGTGACATGT 780
GATTTCTGGC TCAGTATACT ACAACAAGGG AATCATAGCC TACAGAAGAC CCTTGAGAAA 840
CACAAAACGG TGTGGTTGCC CTGTGGAGTT TATTCACCTG GGGTTTGTCC TCAGCACCTG 900
GGAAGCATCA GGAATACACC AGCTTCTCAG AGGCAGGGGA TAAAAACAGT CTTGTGAAAT 960
ATTCTCCTTC TCCTTCCCAA AAAAGTACCT GTGGAAGCTT AAAATAATAA TTAAAATAAT 1020
CTCAGAAACC TTGAGCTAAG GCTGGATTCA GAAAATTGTG TACACTCCTA CATGTACACA 1080
GAACTTAGAG ACATCTTTCT CATCTCCTTC CCAAGAGAAA TAGATCTGTG GCTATCAGCA 1140
CTCATTAATT AAATTAATTA TTTATCATAC CTTCAACAGA ATCAATTGTC TTTTATAGAA 1200
|
