| Tag | Content |
|---|
EnhancerAtlas ID | HS138-10287 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr12:102929330-102930990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:102930006-102930024 | GGAAGGAAGGAAGGAAAG | + | 10.53 | | EWSR1-FLI1 | MA0149.1 | chr12:102929998-102930016 | GGGTGTAAGGAAGGAAGG | + | 6.73 | | EWSR1-FLI1 | MA0149.1 | chr12:102930010-102930028 | GGAAGGAAGGAAAGAACA | + | 6.83 | | EWSR1-FLI1 | MA0149.1 | chr12:102930002-102930020 | GTAAGGAAGGAAGGAAGG | + | 9.25 | | Sox3 | MA0514.1 | chr12:102929406-102929416 | AAAACAAAGG | - | 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 |
| GH12I102534 | chr12 | 102928201 | 102930614 |
|
Enhancer Sequence | GAGGGCAGCG TGATGAAGGG AGGGCGCCTT GAACTGGTTC TAATGCCTGC TTTTAGGTAA 60
TCCCTTTCTC ATCTGGAAAA CAAAGGGCTT GGGGGCCCCT TTAAAAAGTC TCTGCTACTC 120
TGATCCCTTT TATTTATTTA TTTTCCTTGA TTACTTTCTC TCCAGTGTAA AGCCATTTCT 180
GTTTTGTGTT TCCTTAGCAG ATTTCAATTC TCCAAGGGCA TTTGGCTCCC TCCCAGCACT 240
AGGCCTAGGC AGGGCTGCCC TTTATGACAA GGTGAACAAA TGTAATAGAG CTGAAGGACC 300
CAGGATGACA GTGTAGGATC TTTTCCCAGG CTCTTGCCTT TGCCTGGCAT ATCAGTACTT 360
AACTGACGAT GCACCAAGCA CCAAACTTCC ATGTAACCTT CAAAGCCCAG TGCCGTTCTT 420
ACCATCACTA AGAAGCTTTC CTTACCATAA CCCTGTGTGC TAGCCACACC TAAGTAAAAT 480
TCATATGGCT GCTACTGTAA TTCATACCTG CTTTCGTAGC TGGGATGTTT CTGGCTTAGT 540
CCTTGTTTAC ACGTCGGTCT TTTCTACAGG CATGTGGGTT TCCTGAATGC AGGAGACTAT 600
GTCTTTATCA CTTTTGGTTT AATAGTGCCT ATTACCTGTT ATACAACAGA AACTCTACCA 660
AGATTTGTGG GTGTAAGGAA GGAAGGAAGG AAAGAACAAA GAAAGCAATC CAATCTATTT 720
GGCTCTTTTC TGTAGTTACA AATTTATAGG AAATCTGCAA AGTGTATGAG TCAGTCCACA 780
GAGCTTCTCC ACTGTGTGAT TGGGTTTTGC TTGGGTCATC AATCTGCCAT TTCCTGACTC 840
TTCCATCACA CACACACACA CACACACACA CACACACACA CACACACACA CACAGAGCCA 900
CAGCATCATC TTTGAGCAAT GCAATAAATT TTATGAGGCT TTATTTCCCT TCTCTTTAAA 960
ACCTAGAGAA ATAGAACAAA GTTCCCTTTT TCTTTCACAA AACTCATGGG TAACATATCA 1020
ATTATTCAAG TCCATTTATA TGTCTATAAC CACCTCTTCT CTCTTTGTTT CCTCTGGAAA 1080
TCTTTACTTT TCATGCACAC ACACACACAC ACACACACAC ACACACAGAG ATATGTATGT 1140
GTATAACATC ACGCAGTAAT ACATTTTTCA AAGCTACTTT TTTTCAACTT TTGGATTCGG 1200
AGAGGACATG TGCAGGTTGG TTACATGGGT ATATTGTGTG AGGCTGAGGT TTGGGGTACA 1260
GAGGATCCCA TCACCCAGAT AGTAAGCATA GTACCCAACA GGTAGCTTTT GAATCCATGC 1320
TCTTCTCCCC CTCTAGTAAC CTCAGCGTCC ATTGTTCTCA TCTTTACGTC CATGTATACT 1380
CAATGTTTAG CTCCCATTTA TAAGTGAGAA TGCCTGGTAT TTGGTTTTCT GTTCTTCTGT 1440
TAATTCACTT AGGATAATTC ACTCCAGCTG CAATCCATGT TGCTGCAATG GATATGATTT 1500
TGTGCTTTTT AATGGTTGCA TAGTATTCCA TGGTGTATAT GTACCACATT TTCTTTATCC 1560
AATCCACCAT TGATGAGCAC CTACATTGAT CCCATGTTTT TGCTTTTGTG AATAGTGCTG 1620
TGATTAACAT ACAAGTGCAT GTGTCTTTTT GGTAGAATGA 1660
|
