| Tag | Content |
|---|
EnhancerAtlas ID | HS176-15452 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:70668670-70670000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr16:70669433-70669448 | AGAGGTCAGAGGTCG | + | 7.55 | | NR2C2 | MA0504.1 | chr16:70669426-70669441 | GGAGGTCAGAGGTCA | + | 8.03 | | Nr2f6 | MA0677.1 | chr16:70669434-70669448 | GAGGTCAGAGGTCG | + | 6.06 | | Nr2f6 | MA0677.1 | chr16:70669427-70669441 | GAGGTCAGAGGTCA | + | 7.42 | | Rxra | MA0512.2 | chr16:70669427-70669441 | GAGGTCAGAGGTCA | + | 6.88 | | SOX10 | MA0442.2 | chr16:70669279-70669290 | TGCTTTGTTTT | - | 6.02 |
|
| | 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 |
| GH16I070634 | chr16 | 70668595 | 70670270 |
|
Enhancer Sequence | TCTGATACCT ATCACCATAG ATTAGTTTAT TGGCCTGTTC TTGCATTCAA ATAGCTGGAA 60
TTATGTAGTG TGCACGCTTT TGTGTCTGGT TGCTTTTGCT CAAAATAATG TTTTTGAGAT 120
TCATCCATGT TGCTGCACAG ATCAGCAGTT CCTTTTAATT TCAGAGTAAT ATTCCACTGT 180
CTGATTATGG CACAGTTCAT ACGTCCAGTC TTCTGTTGGC AGATATTTGG ATGGTTTTCA 240
GTTTTAGAAG TGCCTATGAT TCATAGTATG AATACAGCAG CAATAGGCAT TCTTGGTCAT 300
TCGTCTTATG GCCATAGAGT TTGATTTTTC TAGGTTAAAT TCTAGGAGTG GGATTGCTGG 360
GTCAGAGTCT AGGTATGTGT TTAACTTTGT TAGAATCGCC AGTCTTCCAA AATGACAATC 420
CCAGCTTATA CTCTCAAGGG TAACGTGGAG GGCCCCATTA CCATGCATCC TGAGAACTCA 480
AACAGTGATT TTCTTGGCGA CAGATATTTT CTTTGCTCCA TAGAGGGGAT AACCCCTCTG 540
CAGAGGTTTC CATCACAGAG CTGTCAAGCT AAACACCCTC CAGCTGCTGC AGCCTACCCT 600
GCTAGTTTTT GCTTTGTTTT CTTTTGTCTC CTGCTGCTCT CAGGAAGCAC AAAGGCCTGT 660
TGGAGGCCCT TTGTCTACTG TCCCAGTACC AGTGTGGATG CTCCACAGTC TGTTCTTGTG 720
CTCTTGAGTC CCCTTGCTAG TCACAGGTCA GAGGTTGGAG GTCAGAGGTC AGAGGTCGGA 780
AGCTGGAGTC CTTCAGCAGA ACATCGGCAG CTTCCTTGAG CAGGAGCTGT TTCCAGTGTT 840
CAAGGGTCCC ATTGACTGGT CCCACGCTGG GTTTCTTTCT TGCCTTCTTT CACAATCAAG 900
TAAGTATTTT GCTCACAGAC CTCTATTGAT AGTGCAAAAA CAACAGCAAA AGGGGAAATG 960
ATTCAAATAT AAAAGAAAAA GCCTACGTTT TTCCAAAACC CATTTTTTTA CTATTAGTAA 1020
TACGAGTGAG TAATTATAAC AATAGCAAAT ACCAAGATAG CATGTACTGT ATGCCAGCTC 1080
ATGTTCTAAG TTTTCTGTAT ATAGAAATCC AGTAAATCCT TACATAGCCC TTTGAGGTCA 1140
GAATCTCATA TCAAGCCCAT TTTACAGATG GGGAGGCTGA GGCAAAAGAG GATCCTCACC 1200
TTGCCCAAGG CAAGGTGGAG TCAGAGTTTG AACCCAAAAG GTGTAGCTTC AGGGTCTGTA 1260
TCTTTTTTTT TTTTTTTTAA TTTTTATTTT TGAGACAGTC TCGCTCTGTT GCCCAGGTTG 1320
GAGTGCAGTG 1330
|
