| Tag | Content |
|---|
EnhancerAtlas ID | HS187-24427 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:135536940-135538370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:135538062-135538075 | TTCTAGAATATTC | + | 7.22 | | NEUROG2 | MA0669.1 | chr8:135537112-135537122 | AACATATGTC | + | 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 |
| GH08I134525 | chr8 | 135537881 | 135538010 |
|
Enhancer Sequence | TGAGGTTGAG AAGCCCTGCC TCACACCATA GCATGCTGCT TCCTGCACTC AGTCCTCTCC 60
TGGTATTGCA CATGTCAGGA TCAGCTAACA TCCTCATTGG TTAATCCAAT GAATACTCTT 120
CACTCTTTAT CTTACCACTA GTACCACCAC CAACACTACT AATAGCAATA ACAACATATG 180
TCTTCCACTA ACTGGGCAGT TACCATGCAT CAGGCACCTC ATACATCAAG TCATGGTTTC 240
TTCACAACAG CGCAATGACA CAGGCATGCT TAGCTTGTTT TATACAGAGG CTTGGGATGG 300
TGAAGTAACC CTACTGAGGT CACACTGGCA AAGTTAAGAA CTGAATCTAA GTCTAACACA 360
CATCCTTAAC CCCAGCCTTT GCTATTGTCC ACTGTGACTT CTCTGCATTA TATGGCGATG 420
CTGACCACAT TCTCCAGTCA AGATCTAGTT TTTCAGGGCT TCTGTGACAC CACTCACTCC 480
TGGTTCTTCT ACCAAGCACC TCTCCAACTC AAATCCCTGT ACAGCCTTCT CATCCTCTGT 540
GTGGAGTCCT AAAGCCTCAC AAACAGTCCC CTCTATATCT CTGATATGCA GGTCCAGTGA 600
TGTCCCAAAG TATCCCACCT CCCCAATATA CATGTGAGCT GAACAAACCA CTAAGATGCT 660
TATACTTAGG CAACGAAAGA GCTGAGCTGA CCACTGAGTG TATCTCAGGC TGCTATGTTT 720
ATGTATTGCT CATTAGGGTA CTCGGGAAGA AATGGAGGAA TTCTGTCCTG ATATCAAGGT 780
TGTCTGGACA AATTATACCA GATAAACCTC ACGGGGATGT GGCCCACATT TAGTCATCTC 840
CCAGATGCAG TTTTGATGCG CTCAATCTCC AAATCAATTC CGTGTCAGTG GAATCAAGAC 900
AGAGCAGTGT TCTATTATTG GGGTTTCTGT TCTATCAGCT GAGGTTGTGG GTAATTTTCC 960
AAAGAGTCAC TAGTACAGAG GCCAACCTGC CAGCCACATG CAGCCCCAGC ACCTCCGCCC 1020
ACTGCTTCCT GGCCCCAACC CTGGTGGAGG CAGAGGAGGG CACCGAGGCA GAAGGCGCCC 1080
GCTGTCAGCA GAAAGACTGG CAACAAACAC TAAATTCTTA AATTCTAGAA TATTCTGCTG 1140
AAAAGACAGC TCAGATGGAT GTTTATTTTC TGAAAGTCAA ACATACTGTG CTGTTTTTTA 1200
GGCAAAAACA AATGAGCTTC TTTCTTGCCC AGAGGATAAA CTTCATTTTT AACTTCCTTT 1260
GTTATTGCTT TTTTAAATCA GATAAAATCA TGTCTTTTCC TTCAATCACC TTTTAAAAAC 1320
CTCCAAGTTA TGAAGACCTC CACTTTTTGT TGTTGTTGTT GTTGTTAAGC TGATGTTGCT 1380
TCTCCTATAA AGACTTAATA TGTGATGATG AACAAAGGCA AACTTTTAAA 1430
|
