| Tag | Content |
|---|
EnhancerAtlas ID | HS182-06832 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr14:99933580-99934720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr14:99934257-99934270 | AGCAGCTGTTCCC | + | 6.92 | | Tcf12 | MA0521.1 | chr14:99934256-99934267 | CAGCAGCTGTT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 99933712 | 99934074 | | chr14 | 99934127 | 99934367 | | chr14 | 99934490 | 99934508 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH14I099467 | chr14 | 99933861 | 99934010 | | GH14I099469 | chr14 | 99934490 | 99934508 |
|
Enhancer Sequence | AAGGAAACTG GTAAAAATAC ATAAAACTTT TGCAGCAATA CAAGGAATTT TTTTTCTGTG 60
ATCAAAAGCA GAAAATTTAA GTGAGGGGAG GGCAGGATGA CAGACAGCTT AAGCACCTTT 120
TCCTATGCTT AAGAAATGTC TTCTTAGAAG AGAAAAAAAT CTCCCCATGG TTCTGGCTCA 180
CAGCCAAGAG CAAGGGCACA GCCTGGACAC AGCACCTCCA CCCTTCTGGG CATTTCAGGC 240
TTCCCATATC TGCGGAGGGC ATCTCTGGAG GACCATCGAA CTTGACCTGA AAATAACTAA 300
AACCACCAAG GAGTCTGGTA ATAAGGACGT TAATCACACT TCCAAATATA GTGGGTCTGC 360
TGGCTTGGCA GGAGGAGACG CAGAAGCATC CTGTCAGCAA TGGCTTAGCT GGCCTCTCCC 420
TTCAGCCTTG CCTGAAAGAC CTTCTGCTGT GGGAGCCTGT AAACGAGGCA AGAACGTCAC 480
TTTGATGAGG AGCTCCAAGA CCCTTTCCCT TCTCTTAACA GTAAGTGAGC CTGGGACAGG 540
GCTGTTCTGC ACCGGCCCTC ACAGGGTGCC CACCAACAGC TACAAAACAG GCTCTATTCG 600
CTCTGCCTGC AGCCCCTCAC CTCCTCCAAA GTCTTCTCTC AGCTATCCAC CCAACTCCAG 660
TTGCTCATTG ATGTAACAGC AGCTGTTCCC TGGAGCTCAG TATTTACCCT CTGCCAGGTG 720
CTGGACTAAG ACAGAGCTCT TCATTTGATC TTCCTCGCAC TTTAAGCAGT AGATACCATC 780
CTCATCTTTC AGATGACATT GTCAGAAAGG TTAAGTCCCT TCTCTTTGTC CAAGGTCATG 840
CATCAGGTAA GAGGTACAGC TAGAATCTGA ACCCAGAACC ACTACCACAC TGCCTCTGTT 900
TAAATACAGA TTTAAAAAAA AAAAAAAAAA AGTACATGGC AGCAGGTCTT CCAGATCAAA 960
TACCATGGGA TATGGCCCCA CACCCCGCCA CAACCCTGCC AGCAGCCACT CAGCCCACAC 1020
CTAGGCAGCT CCAGCCACTT CCTCCTGCAC CTCCTGAACG AGTCCTCATG GTTAGACCCT 1080
AACACTAGTC TCGTACATCT CCCTGCCCAA GCCTGTCCCT GCTGCTTAAA TCTACCCTCA 1140
|
