| Tag | Content |
|---|
EnhancerAtlas ID | HS187-22228 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:170267720-170269080 |
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 | AGGTTTTGTG TGAAACCCTC ATGCTTTATA CACAGGTTTT GCTGTCCTGT GGTTGTCCAT 60
CAGGTTCTGG GAATTCTGAG CTGGAATGAG GCACTCCAGT AGCGTCTTCC CAAGGGTAGA 120
CCACACAGCA CACGAAGCCC ACCAAGCCTG CACCGCCCAC ACAGCACGGC CCCTCGCTGC 180
AGACCTGCTG CCCTTGTGGG TTTAGGCCTG GTGCTCCCCT CTCACAGGGC CGTGCCTCAG 240
ACCCCACATC CGCGCTGCAA CCTGGAATGC ACCTGCCGCA TGGTGTGAGA GGCGTTTTGT 300
GGGAGACGCC CAGGGCAGTA CCTGCACTGG AAAATACTCA GTGGCTACTG GGCCATGCTG 360
AGGGGCCTTT AGGACATGGA GCTGGAGCTG TGGAGGGCTG GGTTTTGGTC CCATTTGACT 420
CTCCCCCATG CCTCATCCTG AAGTTCTTTA ATCTTGGTCT GATGTTTAAA GTTGGGACAG 480
CCCCTCCTGT GACCTCGGAG GGTTCTGGCA ACCAGGTGAG CTGGTGTGTG TGTGGGAACA 540
GCATGGAGCT CTGTGAAATA TCAGGCGTCT TCCCCGCCAT GGGGCATCGT GGTCAGTGTG 600
TTGTAGGGTC AGTTGACCAC TTGGACACCT GGTTATGACC ATTTCAGCCT CTTTTGGAAA 660
CATTCTGCTT TTATTCCCAT TGGCAAACAA ACTTGCTCAG AGGTTTTATG TGACAAGCTA 720
CAGGCAGCGC TGGAGTGTGG TGTGCCAGCA TGAGAGGGTG TGAGCAGGGG GCACGTTTTC 780
TCTGGAATCG TGCATTATAG GAATAAATCA TGTGTGTGTT TGCACCTTCT CACCCCTATG 840
TGAAGATGAA ACTTTAGTGC TTGAGGTTAA AAAGTGTCCT CATGAAGGAG TCTGGCTCTT 900
TCCGCCCTGG TCTAGAAAAC AGTTTCCCGT GAAGGACCAG GGACTACAGA TTTCCGGCTT 960
CGGGGCCCTA CGGCCTCCAC CCCCGCCATG CAGCTCTGCA GCTGTAGCCT GAAAGCAGCT 1020
GCAGCTGCCG CGCGTAAGGG GTGGCTCTGG GCAGGAAACC ACGTGCGAAC CGCCCCACGG 1080
CAGGGTGCGT CCCACAGAAG GAGCAGTGTG TTCCGTCCCG CTGCACGGCC TGCGAGGGAT 1140
TTCCATGGTG AGGGTGAATC ACGAGGGCTT CTTGTGGCCT GGTCTGTCTT ACCTGCCTCT 1200
CCTTCATGCA GGCTATTTTT TTTTTAAGCA AGGAAAGAAT AACTTTATTG TAAGTATTAA 1260
TTAATTAATT AATTAATTAA TTAATTTATT TATTTTTGAG ACAGAGTCTC CCTCTGTCGC 1320
CAGACTGGAG TGCAGTGGTG GGATCTTGGC TCGCTGCAAC 1360
|
