| Tag | Content |
|---|
EnhancerAtlas ID | HS184-30441 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:134123980-134125420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:134124802-134124823 | AGAGAAGGGGAGAGAAGGGGA | + | 6.21 | | ZNF263 | MA0528.1 | chr8:134124751-134124772 | GAAGGAACAGAGAGAGGGGGG | + | 6.36 | | ZNF263 | MA0528.1 | chr8:134124792-134124813 | AGAGAAGGAGAGAGAAGGGGA | + | 6.4 | | ZNF263 | MA0528.1 | chr8:134124795-134124816 | GAAGGAGAGAGAAGGGGAGAG | + | 7.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 134124116 | 134124802 | | chr8 | 134125113 | 134125200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I133111 | chr8 | 134124060 | 134125911 |
|
Enhancer Sequence | TCATGGTCAA AATATTTAAA AGTCGCTGAT ATGATGAATA TTCACAGATT CACCATTCAG 60
ATCTCCCAAT TTCATATTTG CTCCAGACTT TTTTCCCCAA TAATCAAAAT GTTATTGATA 120
GAATGAGAAC AAAGCCCTCT TTGCATGCCC TCCTGGCTTC GGTCATCCTG AAGGATCAGT 180
TAGTCCACAG GGTGGTTCAG CCTTGCTTCT CGTTCAGCCG GGTGGAGAGT CAGCCATCCC 240
ACCAGAAGGG GCTGTGTTCA CCCAGGAGTG GCTACGTTCA CCCAGGAGGG GCTGTTCCCA 300
CCCAGGAGGG GCTGTTCCCA CCCAAGAGTG GCTGTGTTCA CCCAGGAGTG GTTGTGTTCA 360
CCCAGGAGTG GCTGTGCCCA CCCAGGAGTG GCTGTGCCCA CCCAGGAGGG GCTGTTCCCA 420
CCCAGGAGGG ACTGTGCTTA CCCAGGAGGG ATTGCTCATT GATGGAATTC TAATCACATT 480
GATGGAATTC TAATCACAGG TCCTGTGTGC TTGTAAATGT TTGGAGAAGC AATTTAAACA 540
CACCAGAGTG TGCTGATAAG CACGTTGCAC CGTTTACATA AGGTCCTAGA AATATGTAAA 600
CACATAGCAC AGGACTGTGC TGGGGCCCAG GAGGCTGGGC CTCACACCAG GGGCTGCATC 660
CCAGACTTTC CCCTGCCCAT TGTCTTCAGA AAGGAGGAAA CTGGGTCCTG GGGGAAGGCA 720
GTGAATGGCC CCAGACTCCC ACAGTGCAGA CAGCAGCAAC ACCAGAACAA GGAAGGAACA 780
GAGAGAGGGG GGAATTTCAG AGAGAAATAG AGAGAGAAGG AGAGAGAAGG GGAGAGAAGG 840
GGAGGGGAAG AGAAGGTGAG GGAAGGGAGA GAAAAGGGGA AGCATGAAGG AAGGAAAGAG 900
AAAGACAGAG AAAAGAAAAT AGAAAAAGTT GCGCCCATCT GGACACACAT CCCCCAGAGA 960
ACTGCGTGCC TTTCCTGGCC ATCCTATATA AAATAGCCCC AGCCCCAGCA TTCCATATCC 1020
TTCGTATATG GCCTTATATT TCTTTGTAGC ACCTGTTCCC TGATATACCA TACATTTATT 1080
TGCTCATTTT CCACCTCTGC CACTAGAACG TGAGCCCCAA GAGACAGGGA GCTTGATCGG 1140
CATGTTTGTG GCTGTTTCTC CAAGCCTGGG GCACTGCTGG CCCTGGTGAA GCGTAACTAT 1200
CTGTATGAAA GTGTGCATGA AGCATTCATA TGATGAGTGA CTGAGTCCAT GAATGAAACT 1260
GAATTTAGCT CTCCTAACAT GACCAGACCA CAGTTACTCA TGAGTTGGCT GAGCAAGGAG 1320
CCCGGGAAAG CAAGTGAAAC TCGGGGGTTT GACCTGTTCT CAGACTGCAA CAATGGTTAA 1380
CCTTAACAGA GCACTTATTA AGTGCCAGGT ACCATTGTAA CTACTTGCCA TAATCCTATG 1440
|
