| Tag | Content |
|---|
EnhancerAtlas ID | HS042-11532 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:122048050-122049080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:122048809-122048830 | TCTTTCTTTCCCTTTCTTCTT | + | 6.08 | | IRF1 | MA0050.2 | chr12:122048786-122048807 | TCTTTCTTTCTCTTTCTTTCT | + | 6.76 | | TFAP4 | MA0691.1 | chr12:122048418-122048428 | ATCAGCTGTT | - | 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 |
| GH12I121609 | chr12 | 122047874 | 122049676 |
|
Enhancer Sequence | TTGATGAATT GGATATTGTG GGGAAGGGTG CAGTCTAGGA AAGTGACTGC AGCGTGACTC 60
CTGGGGTGAT CAGAACTACA ATTTCTCCAG CTTCTCTGGG GCCTCACAGA GCCACACTGT 120
GTTTGACAGG CTGTTCCCAG GATGCGGGTG TTTTTATGTG ATTAGGCTGG AACTGTTCTC 180
TGGGAAATAA ATGCCCTCAG TCTAAAGGGC TTTTACGAGC CAGGGCAGGG GATTAAAGGC 240
GGCCGGGCTG TGGAGAAATC CCAGGGTTAG GAGACAGCTG AGCATGGAGA CTTTTAATCT 300
AAACCTTAAA CGTTTTTATT TTCCACTCCT TGAACTCAGG GTGTCACTTT AAATACATGT 360
TTGGCAACAT CAGCTGTTCT ATTTTTCTTT TTAATTATAC AAAGCGAGAT CCTGGAAATG 420
GCTCAGCCCC AGGCTGGGGG AGGCAAGGGA AGTTTGGCAA TGGTAGGAGG CAGAGAAACC 480
AACTAAAAAT CTAGTGGATT TGAAATCCTT TTGAGGGAGC ACAGAGGCCA AACTTCGAGC 540
CACCCTGAAC TTGGTAAGAG CTGCCCTGAC TCAGGATTTC TAAAAGGAGA CCGACAGACT 600
CACCAGCTTA GAATGGAGAG AGGACAGATG GACACGTCTC CAAGACAAAA ATATCACCAG 660
CCCTAGCACT GTTCCTGTAC CTCGAATTTA TTCCCAGGCC CTGTCCTGTT AGCTCAGCTC 720
TTTTCATTTC TTTTCTTCTT TCTTTCTCTT TCTTTCTTTT CTTTCTTTCC CTTTCTTCTT 780
GCTCTTTCTT TCTTTTCTTT TCTTTCTTTC TCTTTTTCTC ATTTCTTTTC CTCTTTCTCT 840
CTCTCTCTTT TTTTTTTTTT ATTAGAGGCA GGGTTTTACT ATGTTGCCCA GGCTGGTCTT 900
GAACTCCTGG GCTCAAGCGA TCCTCCTGCC TCAGCCTCCC AAAGTACTGG GATTACAGGT 960
GTGAGCCACT GTGCCTGGCC CTGTTACCTC CTTTCATCCT CTGAGCAGAA AACAGCTAAC 1020
TAGGTTGTTC 1030
|
