| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00382 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:11443350-11444940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX2 | MA0700.1 | chr1:11443674-11443684 | GTTAATTAGT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 11443709 | 11444800 | | chr1 | 11443705 | 11444695 |
| Enhancer Sequence | CAGGCTCTCT TTTTTACCCA GGCTGGAGTG CAGTGGTGTG AACACAGCTC AGTGCAGCCT 60
TGACCTTCTG GGCTCAAGCA ATCCTCCCAC CTCAGCCTCC TGAGGGACTA TAGGCGTGTG 120
CCATCATGCC GGGCTAATTT TTTATTTTTT GTAGAGACAG GGTCTTGCTA TGTTGTCCAG 180
GCTGGTCTCA AACTCCTGGG CTCAAGCAAT CCTTTCACTT CGCCTCCCAA AGTGTTAGGA 240
TTACAGGCAT GAGCCACTGC GCCCAGTCCA CACTGGTCCG TGATATCAAT AAGACACATT 300
GGCCCATTAT ATCAATGACA TCACGTTAAT TAGTCTGGAT GGGCAAGAAG TGGCAAGTGA 360
TTTGGAAGCC TTGATAGGAC AGACATGCTT CGGAAGGTGG GGACTCCCTA TCAGTGAAAT 420
TTTTAGTACA GTGGTTTGGT TTGGGGCACG CCAGGACATC TCCTCCAAAG GAAACCACAA 480
GTTGTTGCAT CTTGCACCTC CCACACATCA GAAGGAAACA AAACATCTTA TAGGCCTTTT 540
TTGGGTTCTT TAAGCAATAT ATTCCACACT TGACAAATAC TGCTGCAACC CATTTTGCCA 600
AGTGCCAAGG ATGGCTGCCA GCACTGAGAG GGGCCCAAGG CAGGAGAGGG TTCTGCAGCA 660
GCTCCAGGCT GTGGTACAAG CAAGTCCCAC GTCTGGAGTC ATGTGACCCA GCAGACGTTG 720
ATAACAGACA TATCTGTGGT GAGAAAAGAC GCTACGAGTT TATGGCAAGT CCCAATAGGA 780
GAATAACAAC ATAGATCCCT AGAGTTCTGG AACAAGGCCA TGCCATCTGT AGTGGAAAAT 840
CATGCATTAT TCGAAAAATA GCTTTAGTGT GCTTCTGGGT CTTGATAGCG GTGGAGCGTC 900
TGCTCAGCCT GGTACAGACA GCTTCGACAT GACACCCTGT GAGCATGGAG AGTCATCCCC 960
CAGAACACAG AGCACACCCC AAATGAATGA CCATACTATT CTATGGTGTT GTGTCTGCAG 1020
TAGGTAAAAC ACGTGGTCTG GAAGCTAAGG GGTGAAAGTA ACAGAGCCAT CACTCACTGT 1080
CATCCTCAGT GACTCATTTA GGAAATTCAT TTCCTGTCCC TGAAACTTTA AGCTTTGTGC 1140
GTCTGAAGAT CTGCTCTGGT TTCCAGATGG GGAACGCTTC ACCAGGGTAT AGAGTAAGAG 1200
CTCCCCCAAA CTTTAACCCA CATCTGCCAC CTGGTCATTT CAGATTCCTT GGACCAAAAG 1260
GCCATGGGAC GAGGGAAGGA GTCACTGTAC TGGCAGGAAT TACTGTCCCT GAGCAACTGG 1320
CAGGAGAAGG TAGGATTGCT GTTACACAAT GAAGGCAGGG AAGATCAGTT TTGGTACCCA 1380
CGTGATCTGT TGGGCTGTCT TTTGTTATCC TCTTGCCCAT TTTTGACAGT AAATGGGTAA 1440
GTGTGGCAGC CATGAGCTGG GAAGGGCACA GTTACCAGGG AGGGGCCAGA CCTGTGAGGG 1500
ATGAGGGTCT GGGTCATCCC ACGAGGTGAA CTCTAGATCA GCAGAGATGC TCGCCGAGGC 1560
TGAGGGGAAT CTAAGATGGA CAGTAGAGGA 1590
|
| |
|
|
|
