| Tag | Content |
|---|
EnhancerAtlas ID | HS138-29012 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr3:188632050-188633440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr3:188632080-188632093 | AAATTAATTATCA | + | 6.12 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38782 | chr3:188631942-188633181 | HUVEC |
|
| | 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 |
| GH03I188914 | chr3 | 188631790 | 188633190 |
|
Enhancer Sequence | ATCTTTCTTT CTGTTTACTA CATAACACCT AAATTAATTA TCAAACAAGA ACTAATTGGG 60
CACAGCCACA TTCTTAGCTT CTCCAAGCCT CAGTTTCTTC TCCTGCAAAA TGAAGATAGT 120
TGTAAAGATT AAACTAAACT GTGTACGTAA AAAGTTCTTT GGAAACTATA GAACAATGCA 180
AATGCAAGGC ATTGTGACCA CAGTTAGAGA ACAGGCTAGG ATATTTGTTG ATTGTCGTTG 240
GTATTATGGA AATTTGCTGC TTTCTTTCCT ATGAGAAGGG TTCTTCCCTT GTCCTGTTCT 300
TATCAGTCTG ACTAAGTCAC CATTTCAAAG CTGACAATTA AAGCTCAATT TCCTTGCACT 360
TTGTCCTAAA GCAGATGTCC TAGAGCTGGG GACCATAATC ATGAAGCGTG TGATGCATTC 420
TCAGAGTTGG AGAGCAGTGT TTCCAGAGAG TCTGAAGATT AGGCATTTCC TCTCATTTTT 480
CATTTTTGTC AGCTTCTTCA TGTTTTCCTT GCTAAGTAAG AAAAGGCCTC GGTTTCAGTC 540
TGTCATTGTA TGACCCTAAA TGAGTCACTT CTGTATTGGG TTGTCTTAGG TTCCTCAACT 600
GCAAGTGTCT AGTCTTCCAC TCACATGCAG CAGAGCAGCT CCACATTTAC TTATGTTACT 660
CAGAGGGTTA CTTCACATAA GACTTTATAA AATAAGTTCC ATTGTTAATT TCTCTAAACC 720
AGTTGGACTA CATCTTTTCA TGTAAAACCT AGATGATCTC TGATACTCTT GGTTTTTACA 780
TGTAGATTCC ACGATCCCTT CCTGGGAAAG TCATGTAACC AACTATAACA TAGGAGCATT 840
AAACATTTTT AGGTAATAGA ATTAGGAAAT AATGGCTGTG TAAGTATCCA TGTGAATTCC 900
TGTCAATAGT TCTCATATCA TGTGCTTAGA ATGATTTCAA TCTGACTGAA TCTTGCCAAG 960
AAACTCATAG CTCTGCTTTC CCTGCAAATA TGAAGATGTG TCAACCTCAA AGAGTTGGTT 1020
AAACTTTCTG TTTCACTCAT ACAAGTCTGG CATCAAATTC ATTTAGCTTT GTGGTGCTTA 1080
CCCATTACCC ATTTGGCAGA TTTCACTAGC CATGTGACAA AGGCATAGTC CAGCTCAGAG 1140
CATGCAGAAT TTGGAATAAT AAATAGTGAC CCTCCTATTG GGGCTCACAC CCAAGAAACG 1200
TCTTATCTTC TGGGGGAAAA CCAAGATTAA GACATTGGTG GCCAGGCACA GTGGCTCATG 1260
CCTGTAATTC TAACACTTTG TTGTGTTGTT TCTTGTTTTT CTTTTTTTAA CTTTAAGTTC 1320
AGAGGTACAA GTACAGGTTT GTTACACAGG TAAATTTGTG TCATGGAGGT TTGTTGTATA 1380
GATTATTTCA 1390
|
