| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13646 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:122047980-122049780 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:122048002-122048023 | AAAGAAAAAGAAAAAGAAAAT | - | 6.01 | | IRF1 | MA0050.2 | chr12:122048809-122048830 | TCTTTCTTTCCCTTTCTTCTT | + | 6.08 | | IRF1 | MA0050.2 | chr12:122047996-122048017 | AAAAAAAAAGAAAAAGAAAAA | - | 6.09 | | 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 | CGAGACTCCG TTTCAAAAAA AAAAAGAAAA AGAAAAAGAA AATGCTAGGG GCTAGAACTG 60
ACTGGGTTTA TTGATGAATT GGATATTGTG GGGAAGGGTG CAGTCTAGGA AAGTGACTGC 120
AGCGTGACTC CTGGGGTGAT CAGAACTACA ATTTCTCCAG CTTCTCTGGG GCCTCACAGA 180
GCCACACTGT GTTTGACAGG CTGTTCCCAG GATGCGGGTG TTTTTATGTG ATTAGGCTGG 240
AACTGTTCTC TGGGAAATAA ATGCCCTCAG TCTAAAGGGC TTTTACGAGC CAGGGCAGGG 300
GATTAAAGGC GGCCGGGCTG TGGAGAAATC CCAGGGTTAG GAGACAGCTG AGCATGGAGA 360
CTTTTAATCT AAACCTTAAA CGTTTTTATT TTCCACTCCT TGAACTCAGG GTGTCACTTT 420
AAATACATGT TTGGCAACAT CAGCTGTTCT ATTTTTCTTT TTAATTATAC AAAGCGAGAT 480
CCTGGAAATG GCTCAGCCCC AGGCTGGGGG AGGCAAGGGA AGTTTGGCAA TGGTAGGAGG 540
CAGAGAAACC AACTAAAAAT CTAGTGGATT TGAAATCCTT TTGAGGGAGC ACAGAGGCCA 600
AACTTCGAGC CACCCTGAAC TTGGTAAGAG CTGCCCTGAC TCAGGATTTC TAAAAGGAGA 660
CCGACAGACT CACCAGCTTA GAATGGAGAG AGGACAGATG GACACGTCTC CAAGACAAAA 720
ATATCACCAG CCCTAGCACT GTTCCTGTAC CTCGAATTTA TTCCCAGGCC CTGTCCTGTT 780
AGCTCAGCTC TTTTCATTTC TTTTCTTCTT TCTTTCTCTT TCTTTCTTTT CTTTCTTTCC 840
CTTTCTTCTT GCTCTTTCTT TCTTTTCTTT TCTTTCTTTC TCTTTTTCTC ATTTCTTTTC 900
CTCTTTCTCT CTCTCTCTTT TTTTTTTTTT ATTAGAGGCA GGGTTTTACT ATGTTGCCCA 960
GGCTGGTCTT GAACTCCTGG GCTCAAGCGA TCCTCCTGCC TCAGCCTCCC AAAGTACTGG 1020
GATTACAGGT GTGAGCCACT GTGCCTGGCC CTGTTACCTC CTTTCATCCT CTGAGCAGAA 1080
AACAGCTAAC TAGGTTGTTC ATGACATCTA TGGGGTACTC CCTACTGTGT GCCAGCTGCT 1140
GGGCTCACCT GCTTACACGT GTTACACTGT TGTAGGCAGT CAGCTATTCT ATAAGTAGGT 1200
GCTATTATTA TCCCCGTTTT CTAGATGGGG AATCTGGAAT CTCCAGAGAG AACGGATGGA 1260
ACCCCCACAC CCCAGTGTTG GGCCTGCACT TCTTTGCCCT TGGACCCCTC CCTTGCCTTT 1320
CTCTAGCCTT GCTCCAGATC ACAGGGTGGC CAACCTTTGG CAGGGTGGCT TCCTGCACAG 1380
ATGGACCAAC TGGAGGCAGT GCCAGGAGCC TGGTGGGTGG GAGGAGCCTG GTGGTGGGAG 1440
GAGCCTGGTG GGTGGGAGGA GCCAGGTGGT GGGAGGAGGG GAATCCAGGG TGTTCCTACC 1500
CCTCTGCCTC AGGTGGGATC TCCAGCTCCA CCTCCCACCA GACAGGTCCA CTGTGGCTCT 1560
GGCTTCTGCC TGAGGACTCC AGTCCCTCTT CGGTACCAGA AACACCACCC CCTGCCTCTG 1620
TCCCTCCAAC CCCAGGGTGA TAGCAGTCCT CCTGCTGGGG CTAACCTGGG GGCTGCCCTT 1680
CCCCTGCCTG CCTTTTCCTG TAAGTCTTCC ATTACCCCTG GAGCAATTCT CAGGATAAAT 1740
GCTCTTAGTG TGGTAACTGT TTGTCCTGGT CAGATTCTCA CAGATATACT ACCTTCACTA 1800
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