| Tag | Content |
|---|
EnhancerAtlas ID | HS138-00298 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:17613370-17614530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 |
|
| | 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 |
| GH01I017286 | chr1 | 17613436 | 17614463 |
|
Enhancer Sequence | CCAGACAGCT GCCCATGCCA CACTGCCTGG TCCCTTCCGG GGCCTGGCTC TCAGGCCTGG 60
AAAGCCCAGG GAGACTAGGA TGAGGCTTGG GTTCTCGTAG GGAAATTTCC CTTCACCCTA 120
TTGTGGTTCC CCTAACACAG TGGGCAACCT TGACCAGGCC TGAGGATAAG GGAAGATACC 180
CAACCGACTC ACCTACTCCC AGCTGGCTGC CTGAAACCCC TCGGAGTTGG ACCATCAGAT 240
GCTGAACTCG TACTCTCTAG CTGAGCACAT AACTTGGGTG AGCCTCAGTT TCCCCCTCCA 300
TAAAATGGGC AAAATAACTG CCGCTTCATA GAGCTTGCAT GGGGATGAAG TAGGGTAACT 360
CACAAGATAT ACTTAGTGTC AATAGCACAG TGCATGGTGC ATAGTAAGTG CTCAGTAAAT 420
GATGACTGCT GTTACATAAC ATCCCCCAGC CCTTCCTCAA GCATCTGCTG TGTAGAACAC 480
TCCTAATCTC CGCGCTTTAA TAGATGACAA AGACCCTTTG AGACCCAGAG GTGAAATGAG 540
GGAGGTAGGG ACAGGACAGC TGTCTTGGCT ACTCTCAGAT CATACCCTGC TTGTCTCAGC 600
TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT GCCTGGACAA GAAGCTGACA AGAAAGCCTG 660
TCTTTTTTGT GGGGATTTGC AGCTCTGGGT GGCCCTGACT CATGCTTTAT TCAGAATTTG 720
GAATAAGTAG CTGCAGGGCT TCCGCAGGCA TTGCCCAACT CTGTGGCCTC CTGCGGCTTC 780
CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA GGATGGCTGG AAAGGAATTC TGGATGGCTG 840
GACAGAGTCC ATGGGACCTA TCACTTCCTA CAAAGTCACT GTCATCCCAA GTCCCCTCCA 900
GCATAATGAC GGCAAGTGCA AGCATTGTGC CAGCAGGTAC TGAATGCTTC CTGAGCACCA 960
TCTGATATAG CCCTCACAGC ATGCCAGCAG GCAGCTATTA CTATTGTTCT CACTTTATAG 1020
ACAGGGAAAC TGAGGCACAG CCACATGAAA GCGCTTGCCC TGGTCACAGA GCTATTAAGT 1080
GGGGGAAACA AATTTGAGCC TAGACACGTG ACCTCTGTAC CCAGTCACAC CAGTGGTTCT 1140
CAACCCATCT ACACATTAGA 1160
|
