| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04566 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:102193110-102194090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr10:102193626-102193637 | GTTTTATGGGG | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I100433 | chr10 | 102193358 | 102193558 | | GH10I100434 | chr10 | 102193621 | 102193810 |
|
Enhancer Sequence | TTACAAATAT CAGAAGAGCC TGTGTGTGAA TGCTTGTGTG TGTGTGTGAG AGAGAGAGAG 60
ACAGAGAGAG AGACTTCACC AGGTGGGAAC AAATCCAAAG GTGCATACTC AGAACACTAC 120
TACAGCGATC CAACCCTGCT CCACCAACAT AAACCGATGT GTCATTGGGT ATAAATATCC 180
TTATTAAAGA GATCAGATCT ATTGATTAAT GCCAGACTCA TGGGTACCAT ATAAAACAGA 240
ACACTTTCCA AGAGATATCT GACAGTGCCT TGTACCCCAG ATAGACGTGT GTTTATCAAG 300
TCACACAGTG ACTTGGAGAC CGCCATAGTT TTACCCTGAC CAAGACTGTC ATAGAGCTTG 360
GCTTCTAACC TCAGCAGAAG GCTTGCTCAT GTCCATGCAC TTAGTCGGTT TATTCTAGTT 420
TCACGAAGTG GAGGTTTTTG ATTTCTAATC TGGCACAGAT GCTCCATCCC GTGCCTTCTC 480
CAGGGATGTT TTCTGAGATC ACCCAGGTTT TACCAGGTTT TATGGGGCGA GAACCTGTCC 540
TCACTTAAAA AGTAAGGAAG TTATGCCCCC TGCAGGACAA ATCGGTAACT GCAGGCTCGG 600
TGATCTGCGA GGACAGTGTT CTGTGCCTTT TGGAGCACTA TATTGTTTCT CTCCACAATG 660
TGGCGCTGCT GTTCTAAGTG TCATTTTAGG GCCAGTTTAG GGTAGGAAAG AGGGTGACAG 720
CAAGAATTAG AAGGTGTAGG GGAGGGCGCC AGGGAAGTAG GGAAAGGAGA TGTTAGGAAG 780
AAAGCTGGTG GGCTACTTCT GCCAGATAGG GCTTCCCTAG CACCCCAAAT CTGATCCATT 840
GCAATTAGGA AAGTTATCTC CTAGTCCAAG GAATTTATCC AGTAGTTCCC AAATCTGGCT 900
GACTGGCAGA ATCACCAGGA GAACATTTTT AAAGATACAG ATTCCCAGAT TTTATCCCAA 960
GAAACTCTGA TTCATAAATT 980
|
