| Tag | Content |
|---|
EnhancerAtlas ID | HS148-00238 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:28431150-28432550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:28431909-28431920 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr1:28431909-28431920 | CATGAGTCACC | - | 6.02 | | ZNF263 | MA0528.1 | chr1:28431385-28431406 | GGAGGAGAAGGAAGCGGAAAG | + | 6.77 |
|
| | 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 |
| GH01I028104 | chr1 | 28431218 | 28432370 |
|
Enhancer Sequence | ATAAAAGACA TAGAAAATCG GCATAGTGAA AATTCCTAGC ATAAAAAAAC TATTGCTTTT 60
ATGTAACAGT TTAATATTCT CCAGGCAAGA GGCAAATTAC AACTTTGTGA AATGGGCTGT 120
GAGCTACAAA ACTAATAAAA ATCATTCAGA GGTGAAAAGA ATGAAAGGTG AGAGAGGCAT 180
TACATGTACT CTGCCTCTGG AATACAATTC CACTTCCCTA CCAAAGAAGG CAATGGGAGG 240
AGAAGGAAGC GGAAAGTAGA AAAAGCTTCT CCGGCTCCCC TGAATAGGAA TCTGGCAATA 300
ATCTGGCTGC TATTTACTAG CATGCAGCAT CCGAGGCACT GTGTTAGTCC TTCATATGCA 360
GCGCCTCACT GACTTCTCCC AAGGGCACAA TTATTATCTA TCATTTGGCT ATATATATTC 420
TGATTCTCTC CACTTTACAG AAAACTGGGG CTCAAGGTTG TTAAATCATT AAGTCGAAGT 480
CCCAGAGGTG GGAAGGGCGG GATCCAAACA CAAGTGTGTG ACTCCAGCGC TGGGGTAGGA 540
GCACCTTGAA GGTGAAGGAG CCCAGCGAGC TGCAGCTTCC TAGTCCAGCC TCACGTCATC 600
ATCCCTGAGA CCTAAGCTCC TCCCACTCAG ATTCCTGAGC CAATCCGGAG AGAGGCCAAT 660
GGATATTGAT AGACTCTGCA TCTCTCCACC CTCTCTGAAC CCAAGAGCTT TGTTTGCAAA 720
CTTGGTACAA AGCACTCAAC TGCTAGCTTC CGAGGTTCCC ATGAGTCACC TCTGCTGCCT 780
GCAAGATCTG GGTCTGGATG AGCCCTAGCC ACCCCTATAC CCCACCCTCC CAAGTTATGG 840
CACTTTGTAA GCCCTGCTTC TCTCTGTTTG TGTCATTTAC CAGGGCTAGA TTTCTCCCAC 900
TCCCATTCTC CGAGACTTAG TAAAGCCTAG TGGTTACATT TAGTAGGGTT ACACAACAAC 960
CCTACTAAAA AGGCATGGTT ATCATTTGTA TTTTTAGGTT GAGGAGCCTG AAGATGAAGA 1020
CTCTTACACA CAGAAGCACA GACTTTGGTC TGCTTCACCA CTGCTTCTGT GTATAAGATT 1080
TAGTTGGGGT TGCTGTGAGG ATAAAATGCA CTAACCTATA TAACGTGTGT GTGTGTGTGT 1140
GTGTGTGTGT GTGTGTGTGT GTGTGTATTA CAGTGCCTGG CACCTCGTAA GCACTCAGTA 1200
AACAATAGTT GCTATTCTCA TTACTTTCAT TGTTCATTGT TATCCCCATC CTATAGTCTG 1260
TCCAGCCTAA CTTTCATCCC CATCTTCTGG TTTGGGGCCT AGATCTCCTG CCTCTTCTTG 1320
TCAATACATA TTTTTTTTCT CTCTAGAAGT GAATCCCAAC TCTGGGAGGA CTCCCAGGTC 1380
ACTGATGAGT CTTCTTCTGT 1400
|
