| Tag | Content |
|---|
EnhancerAtlas ID | HS007-14807 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr6:116549960-116551180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7.21 | | RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 7.24 | | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.93 | | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7 | | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.55 | | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 6.82 |
|
| | 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 |
| GH06I116228 | chr6 | 116550108 | 116551187 |
|
Enhancer Sequence | TACCTCTAAC TGCTTTACCT CCATTTCTGC TACCTTTCTC TTTTAATGTT GATATTCCCT 60
AACATTCTGT ATTTGGCTCT CCTTTCTTCT CCTGTTGTCC TTCAGCTCTC TACCACTGGG 120
AAGCTTTTAA CTATCATCTA TATACTGATG GTTGACATTT CCTTGTCTCT GGGCTTCACA 180
TTTCTCTGAC CTTCAGAAGC CCATTTCTAT CTGTCTTCTA AAATCTTCAC ATCCCACAGC 240
CCCAGGGTGG CAGGAAAGTT GATGTGCTTG CAACAGCTCA TTAAATCCCC ATCCCATTTT 300
AGCATGCCCC TCTTCCCATA TTCCATAATT ACATTTTAGT TACTTTTCCA AGCACAGACT 360
TTAACCAAGC TAGTAAGCAA AAACCACAAT TACTTTTGCA CTAACCTAAA AAATCAGTCA 420
TCCTCATTTC TTCCCTCCCT TTTAAGTTGT CCTTCTGTTT TCTCAGGTTT GTCCTCACTA 480
CATTCCCACC ACTGCCCGCA TCATCCCTTG TGTGAAATGG CACAATATTT AAGTCATTGC 540
TCCAAATGGT TAAAGTAAAG TTAATGCAAC TGAGCTGGCT GGGATGGAAG GCACAGCGAG 600
CCAATCACGA AACACAGCAT GGCCTTAGCG AGTCGCACAG GTTTGACGTC AGCGGTTGTC 660
ATGGTAACAG GGGCAAAGAT GCTGATGCCA GTGTCAGTCA GGACTGAGCT CCTCCCTCCA 720
GTCTGATTCC TGCCAGTGCT TAAGGATGTA TGGAGGGGAG AAGCGTCTTC CAAGCAAAAT 780
CTTCATCCTC TGTTCTCTAT CACGTGCAGT GCGTCACCAG ATCCTCGCCA GTGCTGAGGG 840
TGGGGATACG GGGGAATCTC TGACTTGCAA GATTAAATTA TCATTGGAGA GGGAACGTGT 900
CAGCCTTGTT CACCGCAGTG TCGCCAATGC TGCTAGCTCA GTTCCTGCCC CTGCCCACCA 960
TTGGGAGAAT CATGAGCCAA CTCTCTCTGT CTCTCCTCTC TCTCTCTCTG TCTCGTCCCT 1020
TGGCCTTAGC TGTCACCAAT ACACTGACTC TGACTCCCAA ATCTTTCCCT GAGACCTGTT 1080
TTCCTGAGTC TCATACGCAG TTCCTCCTCC ACACTAGGCA GCTCCACTCA GTGTTCTGAT 1140
ATCAAGCTTG AGATTCTCCT TCCGCCTAGA AACCAAAAAC AACCAAACAT GCCGGTCACC 1200
TTGTGTGTAT TCTTTACTTA 1220
|
