| Tag | Content |
|---|
EnhancerAtlas ID | HS109-20419 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr6:170267790-170269300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | GAATTCTGAG CTGGAATGAG GCACTCCAGT AGCGTCTTCC CAAGGGTAGA CCACACAGCA 60
CACGAAGCCC ACCAAGCCTG CACCGCCCAC ACAGCACGGC CCCTCGCTGC AGACCTGCTG 120
CCCTTGTGGG TTTAGGCCTG GTGCTCCCCT CTCACAGGGC CGTGCCTCAG ACCCCACATC 180
CGCGCTGCAA CCTGGAATGC ACCTGCCGCA TGGTGTGAGA GGCGTTTTGT GGGAGACGCC 240
CAGGGCAGTA CCTGCACTGG AAAATACTCA GTGGCTACTG GGCCATGCTG AGGGGCCTTT 300
AGGACATGGA GCTGGAGCTG TGGAGGGCTG GGTTTTGGTC CCATTTGACT CTCCCCCATG 360
CCTCATCCTG AAGTTCTTTA ATCTTGGTCT GATGTTTAAA GTTGGGACAG CCCCTCCTGT 420
GACCTCGGAG GGTTCTGGCA ACCAGGTGAG CTGGTGTGTG TGTGGGAACA GCATGGAGCT 480
CTGTGAAATA TCAGGCGTCT TCCCCGCCAT GGGGCATCGT GGTCAGTGTG TTGTAGGGTC 540
AGTTGACCAC TTGGACACCT GGTTATGACC ATTTCAGCCT CTTTTGGAAA CATTCTGCTT 600
TTATTCCCAT TGGCAAACAA ACTTGCTCAG AGGTTTTATG TGACAAGCTA CAGGCAGCGC 660
TGGAGTGTGG TGTGCCAGCA TGAGAGGGTG TGAGCAGGGG GCACGTTTTC TCTGGAATCG 720
TGCATTATAG GAATAAATCA TGTGTGTGTT TGCACCTTCT CACCCCTATG TGAAGATGAA 780
ACTTTAGTGC TTGAGGTTAA AAAGTGTCCT CATGAAGGAG TCTGGCTCTT TCCGCCCTGG 840
TCTAGAAAAC AGTTTCCCGT GAAGGACCAG GGACTACAGA TTTCCGGCTT CGGGGCCCTA 900
CGGCCTCCAC CCCCGCCATG CAGCTCTGCA GCTGTAGCCT GAAAGCAGCT GCAGCTGCCG 960
CGCGTAAGGG GTGGCTCTGG GCAGGAAACC ACGTGCGAAC CGCCCCACGG CAGGGTGCGT 1020
CCCACAGAAG GAGCAGTGTG TTCCGTCCCG CTGCACGGCC TGCGAGGGAT TTCCATGGTG 1080
AGGGTGAATC ACGAGGGCTT CTTGTGGCCT GGTCTGTCTT ACCTGCCTCT CCTTCATGCA 1140
GGCTATTTTT TTTTTAAGCA AGGAAAGAAT AACTTTATTG TAAGTATTAA TTAATTAATT 1200
AATTAATTAA TTAATTTATT TATTTTTGAG ACAGAGTCTC CCTCTGTCGC CAGACTGGAG 1260
TGCAGTGGTG GGATCTTGGC TCGCTGCAAC CTCCACCTCC CGGGTTCAAG CAATTCTCCT 1320
GCTTCAGCCT CCCGAGCAGC TGGGACTACA GGTGTGTGCC ACCACGCCCA GCTAATTTTT 1380
GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCAGG ATGGTCTCGA TATCTTGACC 1440
TTGTGATCCC CCCCTTGGCT TCCCAAAGTG TTGGGATTAC AGGTGTGAGC TATGCGCCCG 1500
GCCTATAAGC 1510
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