| Tag | Content |
|---|
EnhancerAtlas ID | HS165-10477 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr3:169476160-169477670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPDEF | MA0686.1 | chr3:169477315-169477326 | TACATCCGGTT | - | 6.14 |
|
| | 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 |
| GH03I169758 | chr3 | 169476561 | 169476710 | | GH03I169759 | chr3 | 169477201 | 169477350 |
|
Enhancer Sequence | TTTGTTTGTT TAGTTTTCTG TAAAGTAAAA TAGCAGTTAA AAGCTAAAAT GCGTGTATTT 60
ACATTCTTAG GCCTGCTACT GACCTTCTTC AAGTGATTTT ACCTCCCAAC GTTTCAGTTT 120
CTCCATTTGC AGAAGGGAGA TAATGGTGGT TGCCTTATCT CACAAGGATG TCATGAAAAT 180
AAGTCAGATA AATTGCTTTG CCCTCCTTGG AGAGGGGCTC TAGAAAGTAA GCATTATTAG 240
ATATGATGAT GAATACCCAC AACTTCAAAG ATATTTTTAA ATTGCCCCCC CTCCGCCCCC 300
AAGTCTTTGA ACATGTTAAG CCTATGAATA GCACTGGGGT AGGTGTTTAT ATATTTCTGG 360
CAAGCTTTCA CCTCTTGTTA AAGCAGTAAA TGGTCTTTGA ACAAACGTAT TTCTCATTCT 420
TTGATAACTA TGCTTCCTTG TTTGTACACT TGAAAGATGA TTATAATCTG GCATATGAGG 480
TCAAGTTGAA CTCCTTGGTG CCATTACAGT TCAAATGTAG CTTTAATTGA GTTTTTCTTC 540
CAAGGTTGAA AATAAGTCAC CCAGTTCACT TTAGCAAACT ACTCGCATTT TTTAAAAAGA 600
TTGTGGGGAA TGTAACTGTT TTTGCAACTG ATATGTATAA TGTTTTTCAT TTTAGTTATA 660
ATATCCTCAT TGATCATACA AAAAAGTCAG TATTTGTATT TCTTCATTAT TGCATTTTTC 720
TGTTTTCCTT AAATTGTTTT TAATAACTAT AATTATGCCT TTTAACACTT ATATAGACAG 780
CCATAGTACA CACATAAATA TCACCAAAGT GAAAACCTAG AGCCCCAAGA CAAAAAAAAA 840
AAAAAAAATG ATAGTCAAAC ATCATCTAGA GAAAGATTCT AGCTGCAGGT GTGCATCAAG 900
TTCATAATTG GTGTTATTTT AAAAATTCAC AAACCATTAG CACTTCCACC CTTCTCCATA 960
TATCTCTTAA CTATATACCC AAGTCAAAAC CACTTCCTGC CAGAGTAACT ACAACATACC 1020
CATCAGAGCG CTGTAAAATC ATTACTTGCA AAGTAAAGAG TAAGACAGAC TTCTCCTCTC 1080
ATTAATAATA CCAGTTGCTG TCATATATAT TACTCATATA TTCTCCCCAC AACCACCCTT 1140
CAAGGGAAGT CTTAGTACAT CCGGTTGACA CATGTGGAAT GTAAAGTTGG GTGACTTATG 1200
CTAGATTCCC TCAGCTAGGT TAGAACAGGG TAAAAGTACA GGACCACAAT AATATCCTTA 1260
TTTCAATGTC TTCCTGTTTC CTTTTTATAT CAAGGAAGAA ATGAGAATTT GAGGCAACAC 1320
AAATGAAGAC CATATATACT TTGATACCTA CCTAGGAGGG GAGATACAAA CCAGAGTAAA 1380
GGAAAAATAT GGGAAAAGTT GCCTCATTTC CACCTAGTGA TGGTGGAACC CTTGGAACCC 1440
TCTTCACATC CCATAACGAC TGACAGAATG GACACTGAAA AACAGGCCCA CCCCTCAGGC 1500
AGAACCACTG 1510
|
