| Tag | Content |
|---|
EnhancerAtlas ID | HS187-16465 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:42597580-42599050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr22:42598900-42598911 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr22:42598900-42598911 | CTGAGTCACCC | - | 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 |
| GH22I042201 | chr22 | 42597726 | 42599470 |
|
Enhancer Sequence | CTCGCCAACA TGGTGAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCC AGGCATGGTG 60
GCAGGTGCCT GCAACTTCAG CTACTCAGGA GGCTGAGGCA GGAGAATTGC TTGAACCTGG 120
GAGGCGAAGG TTTCAGTGAG CCGAAATTGT GCCATTGCGG TCCAGCCTGG GGGATAGAGG 180
AAGACTCAGT CTCAAAAAAA AAACAAAACC AAACCAAAAA AACCCAACTT TACTACCAGG 240
CAGATTCTTT TCTTTCGCTT TAGATAATCG CTATCAAAAC TTTGTCATCT CACTAGAATG 300
TTAATGCTTT TACTTAACAT GCAAGGTAGA TTTTAGTCCC TCCCTTTTGC CTTCTGTCTT 360
TTGAGAGATA TAATTCCTGA GTGTGTTCGT GTTGGCTGAT GCTATTTCAT AAGACATAAT 420
ATTAATACTG CACCTGAAAT ACCTCACACC CTGCCACCCT TCCCCCCGCA GCAAACTTGA 480
GTTTCCAACA AGAGTAAAAA GGAGATAATG TTTTTATTTC CACCAAGGAC AACTTTCAAA 540
GAGATTAAGT TCTGAACACC CCTGGCAAGA TGAGCTAGCT GCACTATGAT GGAACTACAA 600
CATAAGCTAT AGAGTACTGA GTGAGCTTGC TAACAGGAAC ACATCTTTAC TAAGACAACA 660
ATGAGGGAGG ACACCATCTG AGGGCGGTCA CCAGTCTGCA GCTTGCATTT CCTCTGAAAC 720
CACCTAACTG TTGAAATGTG CCAAACACTG CTCTAAGCAC TTTCCAAAGA GCAACACATT 780
TAATCCTCCT AACATACCTC TTTACTGTAG GTGCTGTCAG TTTTCATACT TTGTATGGTA 840
AGGACAGTGA AGCACAGAGG TTAAGTGACT TGAGCTAGTG ACCTCGCAAG GAAACAACAA 900
GTCCTGGAAT TCATATGAAG CAGTGTGACT CTGGGGCTCT CACCCAGGCC TCCCCTCTAC 960
ACAGCTGTTG AGGAGAACGG CAAAAGCCAG GACCTTCCGG GGCAAGTGTT TAGCTGCCTT 1020
GATTTTCTCT TCTCATACGT TTTTCCAATA AATTGGACGA ATCTGATCTG CAGTAGCAAG 1080
CCTTGAGGGT CCCGCGAAAT TGGCCTTGGC TTGGGGTGCG GAGGAGGAAC CTCCATTTTC 1140
CTGAAACAGT ATTGGATGAA GCAAGCCGTA TCTTTTGGAA AAATCGAAGC CCTAGTGCAG 1200
GACCTGTGTG CGGCAAGGCA TTGCTTTCTG CAGAATCACA CAAACTTTCC TGCATGAAGT 1260
TCAGAAGCCT TGACATAGAG CTTCTCTAAC CACACACCAG CTAAGGGGCC GAGGCTGAGG 1320
CTGAGTCACC CTGCAAGTTC CCTGACAGGA GTTTAACTTC ACATTTCAAC TGGTTTTCCA 1380
GTAGAGACTC AAGATATTTG TTGAATTGAA AGGGATGCCT GCTTTTACAT ACTATTTGCT 1440
GTTAGCTCTT TTAACAGATT AGCAATAACT 1470
|
