| Tag | Content |
|---|
EnhancerAtlas ID | HS064-02376 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr11:18250000-18251430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SNAI2 | MA0745.2 | chr11:18250992-18251002 | TGCACCTGTT | - | 6.02 | | SPIB | MA0081.2 | chr11:18251264-18251276 | CACTTCCCCTTT | - | 6.07 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 18251178 | 18251348 | | chr11 | 18250494 | 18251373 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I018228 | chr11 | 18250521 | 18251725 |
|
Enhancer Sequence | CATCAACACA TTCCCCTAAC TGGTGTGAGG AACAGAGAGA ATGGCCATGT CATTAACTGA 60
AATGGAGAAA CCTGGAGTGT GAAGAGTTCT GACGGGAAAA CCCGAGTTCA TTTTGGGACA 120
CGTTAAGTTT GAGATATCTG GAAGCCAGCT ATGTAGATAT GTCAAGTAGC CAGTTGGATG 180
TACAAGCATG GAGCTCAGAA ATGAGTTTTG CAGGGGGAGA TATAATTTTA AAAGCCATCC 240
ACATATAAGT ACTATTTAGA CTTGTGAAAG AGAGCATAGA GAAATAAAGA ATGGGGGCCC 300
AGAGCCAAGT CTGAAGAACA CAGAGTTTGG GGAGATAAAA AAAGTCCCAG CTAAGGAAAT 360
AAAGGAGAAT TGAGGTAGAG GGTAATATTA TGCTACTTAG AGCTGATGAA GGAAAGAGTA 420
GTATTATGAA GCCAAGAGAC CAAATATATC AGGAAGGAAG GGGAAGGCAA CTGCGTTGAA 480
TGTTGCTCAC AGAGCTACTG ATATGAGAAA AGAGAGATGT TCATTGTTTT TGGCAGCATG 540
GAGGTCAGTG GTGACAAAGG TATTTTGCTG AAGTTGTGGG GACAGAAACC AGGCTGGAGT 600
GGGTTAACAT ATGATCAGAA GTGAAGAATC AGAAGGTGTG TAGATGGGCA ATACTTTCAA 660
CAAGTTTGAC TTATTAAGAG GAAGAAGACA ATGTGCAAGA GTGAAGAGTA ATGTGGGTTG 720
AAGTGTAGGT TTTCAATGGG ATAATCTAAT TCAGAAAGCA ACTACTGAGT GCCTGGACCC 780
TGCTAGGCAT TAAGCATGCA GTGATGAACA AGATATGGTG CCTGTTCTCA AACAAGTCAG 840
ACATTTCCCC AAGCATAAGG GCTCACCTGG CCATTTAAAC CAAGTGCTGG AGATCCACGA 900
AGAAGAAAGG GGTCTCCACT GCTGAACCTC TTGGCCTTGT TCAGTGTATC ACAGGTTCTG 960
AAGTCAGACA AACCAGCCTG CAGTCCTGGC TCTGCACCTG TTACATATGT GACCTTGGAG 1020
AAGGTCCTAA ACACAAACCT CTCTAAACCT CAGTTTATCC AGCTGAGAAC ATCAAAGCCT 1080
TCTCTGCAGC TTAAATCAGA TAAAGTATTT AAACTGTAGG GCACAGTCTT GCAATTGCAA 1140
TTAAAAATGG CAGCTATTCT AATTACTATT TGCTGACTTC CCATACCCCA GCAAAATTTG 1200
GATTGCCACC AGTGTGTGCT TCTGTTGAGG CTCTTACTAA ACTGTGTTGT CTATCTACAT 1260
ATCTCACTTC CCCTTTAGGA CAGGAAGTAG AATTTTATTT GAACTAAAAG CCAACGAAAT 1320
GCCGGCCAGG TGCAGTGGTT CAGGCCTACA TTTTCAGACC CTTGGCCAGT TGAGCCCATG 1380
AGTTAGCCCA GCCCGGCCAA CATGGTGAAC CCCCTTTTTT ATTAAAAACC 1430
|
