| Tag | Content |
|---|
EnhancerAtlas ID | HS150-00287 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:41780850-41782370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:41782015-41782025 | ATCAAGGTCA | + | 6.02 | | RORA | MA0071.1 | chr1:41782104-41782114 | TGACCTTGAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 41780949 | 41781152 | | chr1 | 41781359 | 41781793 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I041314 | chr1 | 41780190 | 41781230 |
|
Enhancer Sequence | TAAAATGTTA TGTATTTGCA AGGCCCATAA TCTTTAAAAG CCCAGTGATG CCAGCTCCAG 60
ACAGCAGCGA GCTCCCTCCA GTATGTTAAT AGATAGTATT AGGGCAATAA TGAAAACACT 120
TGAGACAAGT AAGCTCCTAT CAAAAGCTGA GTAATAGGGC TTTGCCGAGT GAATCACAAT 180
GCAGAAGAGA TTAAGACGTC TGCCGTTGTG CAGTGTCTAT TCAGACTAAC AGCTGCTCTG 240
TTTCTGATTA AAATGGGGTT GGGGAGACCT TTTCGAGCGA GTCCCCTTTT TATCCTGCAC 300
TGTCCTCACC CTTCCCACCT CCACCTCCAA GCACAGGCAC CTTTATTTGC ACTTAACTAC 360
TGCCATTCAT AAACACACAC ACACACACAC ACACACACAC ACTGGAGTCT CAATCATGCA 420
TTGCATCATC ACACACACGG AGCCTCAGAA GCACACACAG CCATTAGCCG ACACACAGCT 480
ACACCGATAT ATCCAAGCAC GTACACACAG TCACATCCTC ACACACCGGT GCACAGTCAC 540
GCATGCAACC AGTCTCTCAC ACACTCATGG CCTCAGCCAG TCTCACACGC GCATTAAATT 600
ACAATCTGTC ACAAACACAG TCTCACATAT GCATTAAATT GCAATCTGTC ACACATATAC 660
TCTTCACACA CAGTCACAAC CAGACACTCA GAGACAATCT AATCAGTGTC AAAAACGCAC 720
ACATACCTGG CTGGTCATAT CCACGTATGG CAAGTCCTTC ATGTGCAAAA TCACACTTGC 780
ACACTCACAC TTGTGATGAC TGTTTGTCAT ATACACACAG CCCTTCACTC ACAGACTGTC 840
ATGTGCTCTC TTACCCACAC ACAGTCACCT TCATAAATAA TCACACATGG CCATGTGCTC 900
ACTCACACAT GGCCACAGCC CAGGCTCATA TGAAGTCATG CTTTTCCTGC ACCAAGATAC 960
AGAGCTAGTC TGCACACCTG CAACTCCCCA GCCACAAGTG TGCATGGAGT GCAAGGCACA 1020
AATACATATA GGCACACAGG CACAGACACC ACTCTGCACA CCCTCCAGGT GGTGACCCAA 1080
GATGCGAGAC TTGACTATGA GCCCGATGGA TGGCCCCGAG CTGGTTCAGC AGCCTCATAA 1140
AAAAGAAAAT CCTCAGAGGT CAGGCATCAA GGTCACCATT CTCCCATCTC TGCAAGGCTG 1200
TAGTGTGAAG GGAGAAATGG AATCGTCTCT GTGGAGCCTA AGAGCACAGA GCTCTGACCT 1260
TGATTGGAAC TGCAGATTTA GACCTAGGAG AACGCAGAGC TGTCCAAGAA TAAGATGGCC 1320
AACTTCAAGA GAGTGAGTGC CCCATCAGTG GAGGTGTGCA CAGGGATGCT GGATAGTCAC 1380
TTGGTAAAGA GGACGAGAAG GGACTCCTGC ATTGTACAGG AGTGACCTGG ATGCCCTGGA 1440
GATCTGTCCC AGTCCAGATT TTGTGTCCTG AGGTCTGTGT ATCCTCTTCC TCAACCCCTG 1500
TCCCATCAGT GACTCCCTTC 1520
|
