| Tag | Content |
|---|
EnhancerAtlas ID | HS170-03721 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr8:74080150-74081980 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr8:74080396-74080410 | ATTCCCTTGGGGCT | - | 6.02 |
|
| | 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 |
| GH08I073168 | chr8 | 74080492 | 74081350 |
|
Enhancer Sequence | GATCACCTGA GGCCAGGAGT TTGAGACCAG CCTGGCCAAC ATGGTGAAAC CCCATCTCTA 60
CTAAAAATAC AAAAATTAGC CAGGCGTGGT TGTGTGTGCC TGTAATCCCA GCTACTCAGA 120
GGCCGAGGCA GGAGAATCAC TTGAACTAGA GAAGCGAGGT TGTAGTGAGC CAAGATCGCA 180
CCAGTGCACT CCAGCCTGGG TGACAGAATG AGACTCCATC TCAAAACCAA AAAAAAAAGC 240
TTCTATATTC CCTTGGGGCT GAAAGGGTAG TTGTCAAATG GCTGCATATT GTACAATCTA 300
CCCAAATGGT GGGAAAGTTA TTCTCTCAGC AGTTTTATGA TGATTGCTGG AAGCCTGTGA 360
GTTCAGACTT CTCAGCTCAT ATGTGGGGAA ACTGAGGCCC AGAGAGGGGG TGATTGGTCC 420
AAGGTCAGAC AAGTCGTGGC AGAGCCAGGT CTGAACCTGG CCTCTCTTTC CTTGGCCATT 480
TGGGCTCCCC TTTGGAAATT CTAGACCATC AGCCCACTAA ACAGGACGAG AGAGAGTCCT 540
CCATCTCTCT CTTTGACATC TGACAGATGG GGCATGTCAG CTGCCGTTTT CTGGTTCAGC 600
TCAGATGGTG AAGGCAGGGG AGGGAAGTGG TTTTCTGGTT CAGCTCAGAT GGCGAAGTCA 660
GGGGAGGGAA GTGGGAGGCA GGGCTGAACG TCATGTGTGT ACATTTCACT TCTTTCTTCG 720
CATTTTGGTT ACATTTAACA ATGTGTTACC TCTTCACAGA GTCATTTATA TCATTTGCAG 780
GAGGCCAAGA ATGACATCAA CATCTATTAA AACCTAACGT TTCATGTTCT TCACTGTAAA 840
CACTCACATT GCTTTGTTTC CAGATATAAA CGCAAAGTCA TTCTCAAGTT GAATGGTTTC 900
TTTCCAAGAA ACTTGATGTT ACTGTAATGA AATTTACCTA ATTAATCTCC TTAAGGAGAG 960
AAGGAATCTG ATGATGACTG TTAATGAAGA CCTCAACGTT CTTCTTGTAA TCAGAGCAAG 1020
GCAATCTACA GATTCGTTGT GGGAGAGACC ATAACTTTCC AAATAAATCT CAGTAAAGCT 1080
TTGCAGACAG GGCACTTGAG TTGCTTCCCC ACTTGGCTGG CTTGCTTTCA GCCTCGGTGA 1140
GCCCTGTACA AACTTCTCCA GAACTCTGGA TGTGTTTCTA TTCACCCATG TCCTTGGACC 1200
CGATGTCTGT GTAAGAACTC ATGGAAAAGG TGAACGAGTC ACGGAGGAAA TCCTTGGTCT 1260
GCCCTACTTC AAAGCCATCC CCTCCCTGGC CACCGTCTGC ACATCGTATG CATGAACCCA 1320
CTCCTCAATA CCTTCTCAGT AGTTTGGTTG CACCAAGCAG TGAGTGTGGA GCAGAGCAGC 1380
AGCTACCCTT TGCCAGGGGC TTCCCTGAAG ACCAGTGAAG CCATCCACAC AAATGTAACC 1440
AAGAATTTCT CCTTGCAAAG GAGCAAAGTG TGTCACCAGG GTATAGGAGG CCACACTGGG 1500
ATGTAAGGAG AACACTCTGT CTGTCTCCTG GTCCCGAGAT CAAGCGGGCC ACAGGAGAAG 1560
TGGAACCCAC AGGGAGGAGC TTTGTGAGAG ATACCACTCT GTAAAGATGT TGAATGAGTG 1620
CTGGCAGTTA TTAACCCTGG AACTGGGGAT CAAACAGATA TACAGGGAAT CACTGGGTGG 1680
AAGCCTGGGA AGGATGGGTC AGAACAGTGT GGCAGAGTTT GAGAAGTTAT AAAGAAAGCT 1740
TAGGGATGCA GCAGGAATCC AGTTTTCAAG GCTGGGGCAG CCAGTCAAGG AGGCAAGTAC 1800
CCAACAGTAA CTGGATCCTC AGCCCCCGAA 1830
|
