| Tag | Content |
|---|
EnhancerAtlas ID | HS073-08482 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:101010590-101011970 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr2:101011876-101011887 | TCTGCCAAGTA | - | 6.62 |
|
| | 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 |
| GH02I100393 | chr2 | 101010337 | 101012478 |
|
Enhancer Sequence | GGCAGAAAAT CATAAGGGCA GGAACTCTGA GTCAGGAATA GATGGTGCCA GGGAAAGTTA 60
CTTTAAGGGC ATATTTTTAA AAGTTCAATT CAAATTGCCA GGGGAAGGGG GGCAAGAGAA 120
AACAGAGAGT CAGGCTTCAC GCTCCAGAGG GCAGGAGCAG GTCTGGGTGA GCTGCAAGCG 180
GGCGGCAGCA GAGCATGGCC CTGGGGAGGA GGGCCGGCAG CAGTGACGAT GACAAAGACG 240
ATGACAACAG TGACATCACA GAACACGGTG TGATTACGAC AGGCCAGAAA CTGCTCTCTG 300
TGCTTTGCCG TGTCTTCACT CACTGAGTCT CACAAAAGCC CCATGAGTGC TCAGGGCAAC 360
AGCAGGACAC TCCTCACCAG GAGCATCTCT GGTAAGGGTT GTAAGGATGG GCAGGTGCCA 420
TGCAGGTCAG GCGCCATGCA AGGCAGGTGG CTGCAGACCC AGGAGGCAAA ATCCAGCTGG 480
TGACCTGACG TGAGCCGCTG CTTTTGCATC CTCACTCCTT TTCAGCCTTG CTCTCCTGGG 540
CCACCTGAGA GCTACTACAT GAGAACTTTC TCATCTATTA GCTAAGGACT CCATCTTCTT 600
TTTTTTTTTT TTTGAGACAG AGTCTTGCTC TGTCGCCCCA GCTAGAGTAC GGTGGCCAGA 660
TCTTGGCTCA CTGCAACCCT TGCCTCCAGG GTTCAAGCGA TTCTCCTGCT TCAGCCTCCT 720
GAGTAGCTAG GACTACACGT GTGTGCCACC ACAGCGGGCT ATTTTTTTTT TTTTAGTAGA 780
AACGGGGTTT CTGTCAGTCA CACTTGTCTT GAACTCCTGA CTTCAAATGA TCCGCCCACC 840
TCGGCCTCCC AAAGTGCTGG TATTACAGGC ATGAGCCACT GCGCCCAGCC TGGACTCCGT 900
CCTTGCTGCG ATCAGGGGTT CCGTCTCTCT ACCCTGCCCA TGCTGGATGC AGCCCACACA 960
ACCACTGCAG GGGCAGCTCC CACAGCAGTG GGCACAATGC CTCTGGGAGA ATCAAATACT 1020
CAGTGAGATC TCTGCAATCC AAATCCCTTT CTTATAAAGA AAAGATCATA TTCAGCAAGC 1080
AATCTATAAA ACTTTACCAA AGCAGAACAA AGTTGCCTGC TAATTTCTAT TAACAAAATG 1140
ATGTCACCTT CATGTTAATG GACTGTGTGA AGGTAAGGCT GGAAATTCTC AGAAGGAACT 1200
GAGAGTTTTG AGGCGCCGAA TGGGGGGTGT AGCTTAGCTG CCTCTCACTG ATGCAAACCG 1260
ACAGCCCTCT GTGGTCCTCC GATCAATCTG CCAAGTACAG AACTCAGCCT GGGGTTTTCC 1320
CCAAATTTCT TCTCAGGTTT ACAAAAACTC CCCCCTCCCC TTTGAGGAAG CTGTTCTCAC 1380
|
