| Tag | Content |
|---|
EnhancerAtlas ID | HS148-11881 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr3:12276660-12278090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr3:12277778-12277791 | AAATTAATTAACT | + | 6.74 |
|
| | 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 |
| GH03I012235 | chr3 | 12277101 | 12277300 |
|
Enhancer Sequence | CCTTGAAAAT AAGTTCTTCA CTGAAAAGCA TTTTAATGAA TGGCACATAT GTCCTTCTAA 60
ATTACCAAAA ATGTTCAAGC ACTGGGGTCA GTTCATAGCT GGCGTTATGG TTGATGAGGA 120
GATTTGTTAG TCATTCTGAA TGCAGTGATA CAAAGATATG CAGCTCTCTG TATGCCTTTT 180
TAGTGATAGC TCATCTGTTG TTCATAAGCA AGACACCCAA ATATCTAAGT GTCAGTCTCT 240
GTACTAATGA ATGGACTTTC TGTTCTCACT CACCTTGAAT TGTGAGAATG AAAGATCACA 300
TAGTGTTAAT TGTTTTCAAT TGCACTTGGC AATTGATCAG GGATCTCTGT AGCCCTCATC 360
ATGTCTTTTA TTGCTCCCTC CTTGAAGTGG CATGCCAAAT AAAGCAAGAA TCTCTTGTGG 420
CATATTTAAA GCCACCCCCA GTTTTTGTAG CACCAGTATG AAGAAGGAGA AAGTTCAAAA 480
TGAGAATTTG TTTTCCAAGG AAGAATGGTA CAAATAAATC AGCTCTCTCG CACAGACTGC 540
TATCAAACCA ACAAACCGAT GCAGCTGCCT AGCCAGGGTA GCTGTTAGGG TGATTTGTAG 600
CTGGGATTTC TTCAAAAGGC AAATCCACAA TTCTATAAGA AGAGGAGTTA AGCTAACGCT 660
CCTAGGTAAT CCAGTAAAGC TTCCAGTAAT TCTGCTTTTT CTCTCCTCTC AGTCATTTTA 720
TTTTTGTCCT TTGTTTATCA TTTGGAATGA TGACTCATAT TGGCTATTGG GCAGCTCTTT 780
GGCTCTCAAC TTTCATTTTA GACATAAGGC ACGCTGCACC CTTTTGAATC GTATGGAATT 840
CCTTTTCTAG TTGAACATGT TATGGCAAAT CCTAGAGACC ATAAACCTAA GTAAGTCTTA 900
TTTACAAACA AGTTATCTCC TTTTATCTCC TAATTTTTTT TCTTTTAAAT ACACTTTAAA 960
AAGGAAGAAA TACTACAGTC TTCCCAAGGG CTAAACTTTT AGCCTCTATC TCAACTCTTC 1020
TTTTATCCAC TTGAATTTCA ATATTTTTTT GAATGGACTA GGTTAAACCT GGATATTAGG 1080
GGCCAGGAAA GAAAGATGCC TCCCTTGGGT TTCCCTTAAA ATTAATTAAC TAGCACTTTG 1140
GTTAGGAATT GACCCTAAAG AGCCTTAATT AATTTTCTTC TGCCGGAACC AATGCTTTAA 1200
TGTTGGTATT TGAAAGCAGA GTAAAACAAA ACCAAAATAA ATAAATGAAA TAAAGAGGTT 1260
TCTGTAAAGA TTTTTAAATG CCAGGCATTA GAATGTCAAC GTTTGCACTA TATTTTGTAA 1320
TTGTTGTCAT CAGATTGAAA AGTCCTTATT AAGCCATTAA GTCTGCATGG TGCTGTGGTA 1380
AGCAATGCAT AAAGAGAACT ACATAGAGAT AATTCCCATT TTGATGGGTA 1430
|
