| Tag | Content |
|---|
EnhancerAtlas ID | HS056-13886 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr6:170268160-170269220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr6:170268974-170268987 | TATTAATTAATTA | - | 6.25 | | Lhx3 | MA0135.1 | chr6:170268977-170268990 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268981-170268994 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268985-170268998 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268989-170269002 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268993-170269006 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr6:170268978-170268991 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268982-170268995 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268986-170268999 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268990-170269003 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr6:170268994-170269007 | AATTAATTAATTT | - | 6.92 | | POU6F1 | MA0628.1 | chr6:170268975-170268985 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268979-170268989 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268983-170268993 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268987-170268997 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268991-170269001 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268995-170269005 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr6:170268975-170268985 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268979-170268989 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268983-170268993 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268987-170268997 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268991-170269001 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr6:170268995-170269005 | ATTAATTAAT | - | 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 |
| GH06I169868 | chr6 | 170268218 | 170269370 |
|
Enhancer Sequence | AAGTTCTTTA ATCTTGGTCT GATGTTTAAA GTTGGGACAG CCCCTCCTGT GACCTCGGAG 60
GGTTCTGGCA ACCAGGTGAG CTGGTGTGTG TGTGGGAACA GCATGGAGCT CTGTGAAATA 120
TCAGGCGTCT TCCCCGCCAT GGGGCATCGT GGTCAGTGTG TTGTAGGGTC AGTTGACCAC 180
TTGGACACCT GGTTATGACC ATTTCAGCCT CTTTTGGAAA CATTCTGCTT TTATTCCCAT 240
TGGCAAACAA ACTTGCTCAG AGGTTTTATG TGACAAGCTA CAGGCAGCGC TGGAGTGTGG 300
TGTGCCAGCA TGAGAGGGTG TGAGCAGGGG GCACGTTTTC TCTGGAATCG TGCATTATAG 360
GAATAAATCA TGTGTGTGTT TGCACCTTCT CACCCCTATG TGAAGATGAA ACTTTAGTGC 420
TTGAGGTTAA AAAGTGTCCT CATGAAGGAG TCTGGCTCTT TCCGCCCTGG TCTAGAAAAC 480
AGTTTCCCGT GAAGGACCAG GGACTACAGA TTTCCGGCTT CGGGGCCCTA CGGCCTCCAC 540
CCCCGCCATG CAGCTCTGCA GCTGTAGCCT GAAAGCAGCT GCAGCTGCCG CGCGTAAGGG 600
GTGGCTCTGG GCAGGAAACC ACGTGCGAAC CGCCCCACGG CAGGGTGCGT CCCACAGAAG 660
GAGCAGTGTG TTCCGTCCCG CTGCACGGCC TGCGAGGGAT TTCCATGGTG AGGGTGAATC 720
ACGAGGGCTT CTTGTGGCCT GGTCTGTCTT ACCTGCCTCT CCTTCATGCA GGCTATTTTT 780
TTTTTAAGCA AGGAAAGAAT AACTTTATTG TAAGTATTAA TTAATTAATT AATTAATTAA 840
TTAATTTATT TATTTTTGAG ACAGAGTCTC CCTCTGTCGC CAGACTGGAG TGCAGTGGTG 900
GGATCTTGGC TCGCTGCAAC CTCCACCTCC CGGGTTCAAG CAATTCTCCT GCTTCAGCCT 960
CCCGAGCAGC TGGGACTACA GGTGTGTGCC ACCACGCCCA GCTAATTTTT GTATTTTTAG 1020
TAGAGATGGG GTTTCACCAT GTTGGCCAGG ATGGTCTCGA 1060
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