| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21663 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:117870000-117871690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr6:117871005-117871016 | AGGCACTCAAG | + | 6.14 |
|
| | 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 |
| GH06I117547 | chr6 | 117868607 | 117872388 |
|
Enhancer Sequence | CTGTTGCAAA ATGTATATAA ATAGTATGTT CATTTTTTTC AGTATATTAT CTGATACTGT 60
GTTAGCAGCA GGTCTGCTTA AACCTAGTCT TGTTGTTATT GAGTCATTTC CTCTCCTTTG 120
ATAACTAGAA CTGAAAGCAT TTTTAACATT CTTCTCCTGG AAGAAATGAA TTACTTGAAG 180
CATGAAAAGC ACACCAGGGT GGTTGTTTAT TTAGCAATTA TGACTGTAGA TTTAAAAACA 240
AGCAAAGAAA CAACACCTCA GCAGCTGCCC GTTTCCTTAG TCTCCACTTC AGAGGGGGAT 300
GCGAAGAGGT CGGCCCAGCT CCGGTGACCA TGAAGGTGGC ACAGGAATTA CAGTGTGAAT 360
GGCTGTGTCA GATGTTTTCG TACCTCAGAT TAAAAATATT GCTGAGGTCA GACGCCACAA 420
TTTTCATGAC TTTCTTCAGA AGTAGCACAT TTTCGTGACT TCCGCTGTCC TCTGAAAAAC 480
AAAGTTATTT GGAACATGTT CATGCAAAAG TGATTCTGAC CAAGTCTAAA TCGAGCTTTT 540
CTACTGACAT GAAACTGTTG GAAACTGATC TCATTTTATA AGAAATGATT TTCCCCTCAA 600
GGAGGCGTCT GTAATTCCAG AACAGTCCAG ACATCAGCTG TACCTCATGC TCAGTAGTTT 660
TTATTTGAGT TTCTTTTGTG AGTTAACTAT GGGAGATTTA ACCTCTTTTG CCAAAGAGGG 720
AAGTGTGTGT GTTTTTTTAA TAGAAAATAT GGACCAAAAA TTTTTTTCCC TGAAGAATGT 780
ATTATAACCC TATTTGTGTG GTTATTACAT CCTGTGAAAT GTATATATGT TAAAATAATG 840
GGGGTGCTGG AAGGTCATGG CAGACTAGCT GCTGGTTAGT GTGGAGGGGA AATGGTTTAC 900
TTTGTAGAGT TTACATGGTT TTATGCGCAC ACTAATTGTA ATAAACTATG CCAAACCAAA 960
CTGCCCCTGA CTCTCACTAG TCAGCCCTGC TCGCTGGGGT GTTAGAGGCA CTCAAGGTTC 1020
AGCTTCTGTA AAAAGGCAGG TGCCACAGTG GAAAGAGAAA GAGCTTGGTG CCAGATTAGG 1080
CCAGACCCCA ATCTACCACA GAAGAGAAGT CTGGCTGCTT CTATAATGAT GAGACTCGGT 1140
TTCCTCATGT TTGAAAATGG TGTTGTCGTG CTTTCTTCCT CCAAAACTTA CTGATAAAAA 1200
TTAGTTGGAA CATTTATCAA AGTGTTGTCT ATAGTAGGTC CTTTTTTCTA ATGTAAGCCT 1260
TCAGTGGGCT GTTTACAGAA TTTTAATATT GGAATATTAG ACCATAAGCA TAGGCCTAGA 1320
TCTACAGCCC TTCTTTACAA TAGAGCTGTC TTCATCTATC ACAGTTCTTC TGCGGCACTA 1380
GTGATCTAAT CATGACCAGT GGGAGAACAG GACTTTTTTT TTTGGATCAT CACTTCCTCA 1440
GGGTAGACTC TGTAGAACAG GTTGGGTGAG TGGAAAGGTC TGATAAACCC TACACAGCTA 1500
AACCTAAACT AGAGGATAAG GGCAGAAAAA TTTTACATCT TTCTTTTTTG GTGTTTTGCA 1560
ATATCAGCAT ATATGATAAG GCGTGAATGA GACAATTCTA ATTGTCTGAC TTATGTTATC 1620
AAATCCTACT GGGAGGCAAA GATTGTATTC TGCCACTTCT TAAATTTGCG GTTGAAACAC 1680
ATTTGCTATG 1690
|
