| Tag | Content |
|---|
EnhancerAtlas ID | HS176-01737 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:95163790-95164970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:95164064-95164075 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr1:95164064-95164075 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:95164945-95164960 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr1:95163939-95163960 | GGAGCAGGGAAGGGAGGGAAG | + | 7.18 | | ZNF263 | MA0528.1 | chr1:95163936-95163957 | GAAGGAGCAGGGAAGGGAGGG | + | 7.51 |
|
| | 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 |
| GH01I094697 | chr1 | 95163099 | 95165326 |
|
Enhancer Sequence | TTTCCCTAAT ATTTCCCTTT AATATTTCTG CCATCATCCT GAGTGAATCC CAACACCCCA 60
TTAATATGTA CAATGACAAT GTGTCAATAA ATAAATCATC TACACATTTT CTTTGACGAT 120
GAAAAACAGT TTCTCCATAG CCTTGGGAAG GAGCAGGGAA GGGAGGGAAG AAAAACAGTA 180
AGGAATGCTT AAGTCCGGGG CTCCTGGTAT AAAGCTGCCC CTAAGTTAAA AGTTGGGAAG 240
AACCTCAAAG AGTGATTAAG GTATCTTTCT ATGTCATGAG TCACCACTGA GAAACATCAA 300
GTGGTGCCTT GAGACCTCCT AGACTTAACA TGCTTCCATA TATAACTAAT AAATTACTAG 360
GAAGAGACTT AGCCCCTTGA TGAATGTCTT ATTGAGACTG GACAACATAA TTTCTGTGAA 420
ATCAATAACC AGCCGTTCTT CCTCACCAAT ACCCTCCCTA GCTAAACATT GTTCATTAGA 480
AGAGATGAAG CAGCTTTGAA ACATACATTA TCCCCCATCT TTTTAGCTAT TGCTGAGAAA 540
TTTTGAGTAC GAATTAATAA CAGGGAAAAG AATCATACTT AAAAGCATGC CGTAAATGGG 600
GCTGTTGAAT TTTTGAGTCA ACCAGAACCA GAACTAATGT CTGCCTATAT GCATGATTTA 660
ATTGCTCAAG GTCACTTTCA AGAAGCTGTG CTAAATGCTG ACAGACTTTG TTGGAATTAT 720
CAGAATTTTT TCAGGCTCAG TCATCTTGGC CTACCTCAGG GAGAAGTCAG ATAAAATGTC 780
AGAGGTCTGA CTACCCAAAC TCCAAGTCAC ATATTTTCTT CCTTGCCTGT GCTCACTAGC 840
TTCTTCTAAA GTCCATTGGT TTTAGAGTCA AATGATCTGC TTTTGAAATC TAACTTCAAC 900
ACTTACTAGA GGCTTAAAAT CATTTAACAA ATATTTATTG AATACCTACT GTGTTACAGG 960
CACTGTAAAC ATTGGTGAGC ATACAGCTCT TTGAGCCTTG GTTTCTTCAC ATATAGATGG 1020
CACTAATAAC CCTTCCTTTG ACAGTAAACC CAGTAGGGGG CAGGATTAGT GATAGGATTA 1080
AGTGACATGG TGGGGCACAG TGGCTCACAC CTGTAATCCC AGCACTTTTG AGAGTCTGAG 1140
GCACGCAGAT CACTTGAGGT CAGGAGTTCA AGACCAGCCT 1180
|
