Tag | Content |
---|
EnhancerAtlas ID | HS095-22422 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:48361930-48363490 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr4:48363342-48363358 | GAGCTTTCCAGGAATA | + | 6.47 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 48362406 | 48362596 | chr4 | 48363150 | 48363424 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I048359 | chr4 | 48361678 | 48363860 |
|
Enhancer Sequence | GAGAGGCTGA GGTGGGTGGA TCACGAGGTC AGGAGTTCGA GACCAGCCTG ACCAACGTGG 60 TGAAACCCCG TCTCTACTAA AAATACAAAA ATTAGCTGGG CATGGTAGTG CGCACCTATA 120 ATCCCAGCTA CTCAGGAGGC TGAGGCAGGA GAATCGCTTG AACCTGGGAG GCGGAGGTTG 180 CAGTGAGCTG AGATCGCGCC ATTGCATTCC AGCCTGGGTG GCAGAGCGAG ACTCTGTCTC 240 AAAAAAAAAA AAAAATAGTG GTTAGTTCCC TTGTAATGAT TGTTCTAAGG GAAAAAGTGG 300 CATTTTGAAA GGCCAGTTTA TTCCTATCAC ATTTTGACAG CTTTATCAAG ATGTTATTTA 360 TATACCATAA AATGCACACG TTTAAAGTGT ACTGTGGGCT GGGCAGGGTG GCTCATGCTT 420 GTAATCCCAG CACTTTGGGA GGCTGAAGTG GGTGGATTAC TTGAGGTCAG GAGTTTGAGA 480 CCAGCCTGCC AACTTGGGAA AACCTGGTCT CTACCAAAAA TACAAACATT AGCCAGCATG 540 GTGGTGTGCA CGCTTGTAAT TCCAGCTACT CAGGAGCCTG AGGCATGAGA ATCACTTGAA 600 CCTGGGAGAC AGAGGTTGCT GTGAGCTGAG ATTGTACCAC TACACTCTAG CTTGGGTGAT 660 GAAGTGAGAC TCTGTCTCCA AAAAAAATTA AAAAAAACAT AAATAGATAA GAAATAAAGT 720 GTACTGTGGT TTTCAGTGTT CAGTAGTTTT TAACGTATTC ACAGAATAGT ACAACCATCA 780 CCATAATTTA GTTTTATAGT ATTTTCAGCA TACTGAAAAG AAACCCTGTG CTCATTAGTA 840 GTCATTTCCC ATTCCTTCTC TCCACCCCCT CATCTATCCC CAGGCAACCA CTGATCAACT 900 TGTCTCAGAT TTGCCTATTC TAGACATTCC ATATCAATGG TATCATACAA TCTGCGATGT 960 TTTGTGACTG GCTTCTTTTA CTTAGCATAA TGTTTGAAGT TCATGTGTAG CATTTTTATT 1020 GCCTCCAACA CATTTTTAAA TGTCTCTTTT CAAATTATAA ATACCAACTC AAAAAATTCA 1080 AACAGGACAA AAATGAATAA AATATAGTCT CTTATTAGAA TGGGCGTAAG GGATAGAATT 1140 TCCTTTTTGA CAGGGCAATC TAAATGTCTA CAAAGATTCT TTCTTAAAAC ATTTTGCATC 1200 AATGTTGTAC ATAGTGGAGA CACTTAATAT GATCTTACTG GAGATGTTCC AGGAAGGTTT 1260 TCCTGAAGAA TTGAAATTTA AGCTGATACC CAATAGAAAA TAGAGAAGAG CTGGATGAAC 1320 TTGAGCAGGG GAGGGTGAGG TAAGCAAAAA AGTGGAATGA AACTTGTTGC AAGGGGAACA 1380 ACATGCACAA ATGACCTAGA AGCAAAAGTG TTGAGCTTTC CAGGAATAGA AATTAATTCC 1440 ATATGGCTGC TATTTAAATA TGTGTGGTGG AGGAAGGTGA GAAATGAAGC TAAAGAAGAA 1500 CTACAACAGT TAAATCATTG GTTAGGTCTC TAGAGCTGTG GGGATCATTT TTAGAAAAAA 1560
|