| Tag | Content |
|---|
EnhancerAtlas ID | HS051-28325 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chrX:40869090-40870580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chrX:40869907-40869920 | TTCTGGAATTTTC | + | 6.17 | | Stat4 | MA0518.1 | chrX:40869527-40869541 | CCATTTCCTAGAAG | - | 7.04 |
|
| | 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 |
| GH0XI041009 | chrX | 40868349 | 40871834 |
|
Enhancer Sequence | AAAAGGAATT TATAACTATC CTGGCATTTA GCAGTTTACA GGGGGGTTTC ACTTCCGTTT 60
TCTCATTTGG ACCATGCAAA AGCCAACTGA GTACAATTCT GCCCATTTTA CAGATGAACA 120
AACCAGAGGC ACAGAGGAGA GGGATTTGCC CGAGGCTACA CAATACCTGT GAGTCACAGC 180
CAGGACTAAG GATCCTGTGA GCTTCTCAGC ACATGCCACT CCTTCCTACA ACACCCTGCC 240
AGGTCCACCA CCTCCGTAAG TGGAGAATCT TAACGAAGGG CGACCTATGC ACGCACCTGA 300
CTTCTGAGCT GAGGAACAGT AGAATGAAGG AGTTATTTTT AAATGGCTTT TACCGAGCCT 360
GTGATGTCAT TTCATTGATC ACGCTGGGAG ATGCGGTGCT GAGTTGTGCT ATGGCAACTC 420
GATTAAGGCT GGGAACTCCA TTTCCTAGAA GCCCCTCCCT GCTGTGTTTC CGGGTTAGAG 480
TTGGCCAAAA GAGAACCTTG TGCAAGAATT GTAGGGCGGA AGGCGAGCAG CAGTCACTGC 540
CCCTGGCAGG TTTCCCGTCA GATACAGTGA AGGACAGAAA CAGAGGGGCC CTGAGAGGCC 600
CTGCAGCTCC CGGTTTATCC GGCTCTCTCC TCTGCTCCCT CCCAGCTAAC ATTTCCTGCT 660
GTTGGCTCTG CTACCCAACA GCTGCCTCGG GCCCACCACC AGGGGCTTGG CTGTCGCCCC 720
ACATGGGGCG GGAGCTACGT AGAGGCCACA GCTCCCATAA ACCTCTCCAC GAACTCCCCC 780
TCCGCGGCCC TGCTTCGGTG GCTAGATGTG CTTTGGCTTC TGGAATTTTC CTGCAAGCTC 840
TGATTTGTCC AACTGCACCA GTGCTTCCGG CAACGGCTAG TGACTCTCTG ATCTTCTGAC 900
TCCTCCTTCC AGACATTCAC TTCCCCAGCT CTTCCCACAG CTGTGAACGG TTTTATTCCT 960
AGAATACTCA CAGTGGCTCT GTTTCCCTGG CTGAATCCTG TTACGATACT TACAGATTCT 1020
GCTTTACATG AAAAACAGCA TAAGAAAAAA AAAATGTTCT GGAGTGTAAG GCAGAATTCC 1080
ACCTGATACT TAGAATCTAT ATATCTCATG TGCTTGATTT ATAGATTGGA TATGTGGGAA 1140
CTAAGGAAAG AAGATTATTC AATGAACCAG TGGAGGAAGA ATCGTGTATG CTTTCAGTGT 1200
AGACCAAACT GGGGAAATAG ATGAGAAAGG AATAACTGAA AAGACATAAC CTTCTTTATC 1260
TTGTTTTTCT AAGCTCAAAA GATGGAAGAG GGGAAGGAAT TGGTAGTGAA GCCATTTTTG 1320
TAGTCTGGAA ATTTTCTGTC AAGTTTTACA TAATTCCTTA GGGCATACCA AAGAAAATAA 1380
TCAGTCCTGT CTACCCTCTA AGTAACTATC TTCTCTTGAA AGAGAAAGGA GTGATTCTTA 1440
TTTAGGAAAT CTAGTTCTTT AAATATAAAA TACGAAATTG AGCCTGGGCA 1490
|
