| Tag | Content |
|---|
EnhancerAtlas ID | HS029-00045 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr1:2230020-2234410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr1:2233877-2233894 | AGGGACACGGTGTCCCC | - | 6.06 | | Ar | MA0007.3 | chr1:2233877-2233894 | AGGGACACGGTGTCCCC | + | 6.17 | | NR3C1 | MA0113.3 | chr1:2233877-2233894 | AGGGACACGGTGTCCCC | - | 6.03 | | NR3C1 | MA0113.3 | chr1:2233877-2233894 | AGGGACACGGTGTCCCC | + | 6.23 | | NR3C2 | MA0727.1 | chr1:2233877-2233894 | AGGGACACGGTGTCCCC | - | 6.08 | | NR3C2 | MA0727.1 | chr1:2233877-2233894 | AGGGACACGGTGTCCCC | + | 6.2 | | RREB1 | MA0073.1 | chr1:2230472-2230492 | TCTATGTGGTTGTTTTGTGT | - | 6.35 | | TFAP2A | MA0003.3 | chr1:2233512-2233523 | TGCCTGAGGCT | - | 6.32 |
|
| | Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
| SE_01499 | chr1:2230890-2232649 | Adrenal_Gland | | SE_10605 | chr1:2230613-2234200 | CD19_Primary | | SE_11303 | chr1:2229194-2235579 | CD20 | | SE_12227 | chr1:2230249-2234208 | CD3 | | SE_16839 | chr1:2230637-2234084 | CD4_Naive_Primary_8pool | | SE_17322 | chr1:2224537-2236334 | CD4p_CD25-_CD45RAp_Naive | | SE_18225 | chr1:2229290-2235668 | CD4p_CD25-_CD45ROp_Memory | | SE_18345 | chr1:2229268-2234646 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19191 | chr1:2229524-2234390 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20385 | chr1:2230482-2234122 | CD56 | | SE_23033 | chr1:2230059-2233784 | CD8_primiary | | SE_31962 | chr1:2230626-2233595 | Gastric | | SE_33669 | chr1:2230327-2233314 | H2171 | | SE_41586 | chr1:2230182-2231307 | LNCaP | | SE_46124 | chr1:2230507-2233519 | Osteoblasts | | SE_54996 | chr1:2230147-2233027 | Stomach_Smooth_Muscle | | SE_55573 | chr1:2231182-2233462 | Thymus | | SE_68719 | chr1:2229029-2232774 | H9 | | SE_68719 | chr1:2232808-2234035 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr1 | 2233200 | 2233593 | | chr1 | 2230836 | 2233000 | | chr1 | 2231691 | 2232185 | | chr1 | 2232428 | 2232896 | | chr1 | 2230678 | 2230895 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002298 | chr1 | 2230106 | 2234390 |
|
Enhancer Sequence | ATACGGGGTC CCGTTTACCA ATGAGGGCAA AGAGACCAGT CTAAGGGGAG GCTGAAAACT 60
CACAGGCAGG CCTGTCTGGC CTTGGGGTCT GGGTGCTGCT TCCAGGCAGA CCACATCCCA 120
GGTGAGGTGC AGACATTCAG AGACAGACGT GGCCGATCCT GGCTGCTGTA TCAACGCGCC 180
CACCAAATGG GGCCTTCTTT GATCATCAGT CAAAAGCAAG AATGTGCCTG TGGTGGGCGG 240
GCGCGTGTGC CAGCTTCCAG GCCGTGGGCT CCTTGGTGCC CAGAGCTCAC CCTGTGGTGC 300
TTGCCCACTA CTCACTCCCG CCTCCCCGGA GTCTTGCCCT GGGGGGTCCT GGTGTGGGAG 360
CTGCCTTCTC TAGTTGGGTG GAGCCTTGCC TGCTGGTGCC TGTGAGCCCT GGGTGGGTGG 420
ATGCCGGGTG GTCGTGGAGG TTCACAGCAG GCTCTATGTG GTTGTTTTGT GTGGATTTGG 480
GGTGTGAATT CTCTCAGCAA AGGCTGACTC AGACCCCAGT GTTCAGAAGG TTCAAGGAAG 540
CGACCGTCAG CGCCGAGTGG CCAGCAGGGC GGGGATGCGG CGTTGAGCCC CGTCATTCAG 600
CTTCAGTGTG GAGAAGGCCC GGAGCTGTGG GCATCAGCTC GGGGACCCGA GTGACTGTCC 660
CTGCCTCGGG GAGGGGGGGG GCCACACGGG CAGGCGGGGC AGCAGCTTGT GCCCATGTCC 720
TCCTCACGGA CTCTGGAAGT GAGAGGCGCT GAGGCCACAG TGGGGGAAGT GGCCCAGCTG 780
ACGACCCGGG CTCTCGGTGC CCTGGGAGGA GCTGTTGTTA GGACATGTGC AGACTGGGTT 840
CAGCCTGTCT GGAGTGGCTC AGGTGCCTGG GGACAGAGGC CAGCTGTAAC CGCTGCTGCA 900
CTCGGTTCTG GATTCAGTGC CCTCCGCCTC TGCGGCGTCT CCCTCGGCAG CTGTCCAGGA 960
CTCCAGCCTC CCTGCCAGGG TAGGGGACAT GGAGCGTCTC CTTGCTCTGG GGGGTTGAGG 1020
TCTTCTGTGT TTGGACCCTG TGGGATCTGG CAGGAGAAGC AGCCCCCACT CATGTTGTGC 1080
CAGGGGCCTG GGGAAGGGAG ATGGCAGTTC TGTGACCTCC AGACTCCCTT TCCTTATTGC 1140
AGGGGATGGG CCAGCGTTTC GCCCTGAGCA TCTGCACGTG TCAGGCAGGA AAGGGTCCCC 1200
AAGGCCTTCT CAATGGCTCT TCTCTGTTCC TGGCACCTTA CAGGCCTGAA ACGCAGGGCC 1260
CCCAAGGGTG GGGTGTGCAT TTTTGGAGAG CGTCTTTTCT GAGACTCCCC CATGGGGAGC 1320
TGGTGGCTTG CTTGTGGCAG TGTACTGTGG CTGCCCAGTC CTCGGCAGGC ATCCACTGCT 1380
GGCTCACCTG TTTGGGCCAC CGCCTCTGCA TAGGTCCTGT GGGCTTTGCT CAGGAACTGT 1440
TCCGTCAGAG GGCCTAGGGT GTCCACAGTC TTGGGCCCGC TATTCCTCAG CCCAGCCCTG 1500
CCCTGCCCTG GCAGGGGGGC ACCTGTCCTT GGGTGCAAGC TCACACGCGT TGCCCGGGTG 1560
CCTGCTGGCC AGGTAGCTTG CCTGGTCATC CTCGGGGTGT GGGGAAGGAC CCCAGGAGGG 1620
GAAGTGGCCG CGGGGCAGCG CGGTGTGTCG TCTGGCCTCC GCTGTGTAAG CTGACAGTGG 1680
CCTGAAGGGC TTTGGGATGG GGCAGCCCCT TGCAGGCCTA TCCAGGCCCA GCCCCATTGC 1740
TTTGGTGTGT CAGGTCCAGA GCCGTGCTCC TGCCTCGTGG CCTGTGGGCT CCAAGGGCGG 1800
GTTTTGAAGC CCCAGGAAGG GTCACACCAG AGGCAAGCGG TCGTAGCTGC TCTTCCCAGA 1860
GTAAGACTCA GCCGTCTGTC ACTGGGTGTG GTTTTGTCCC TGACCGACAG CTGACACTGG 1920
GGCCCCCAGG GGCCTTGGTA GGGCGGGTGG CATCCCAGGC CTGAAGACGG CTGTCTGCTT 1980
CCTGGGGCTT TGAGAAACCA ATACTGCTCA GGTGACAGTC CCTCTGAGAG TGTCACTTCC 2040
TCCGCCCACA GGGGCGCAGA CACCTTCTAT TTTACACGTT TCTCTCCGTT TCTCTGATGC 2100
TGCAGAGAGC CCGCCCTGAG AGCCGGGAGT CGCCTGATGA GGGGTCGGCA GGGGTCTTAA 2160
CGGAGTCATG TCTCCGAAGG CTCGTCCTGG CTCCCTGAAG ACCAGGAGCG TCCCTGGCCC 2220
CAAGGATGGC CCTGAGCCCA TCTGCCTCAA CCCTCCAGAT CTGCAGGGTC CTCGGCCACC 2280
CCCCACTGAG CGGATTGGGC TCGGGGCCCC GGGCCTACGG TCCTCCCGCC ACCTCCACGG 2340
GGCGGCTGTT GGGGCCCCAC CAGGCAGAGC CGTGTTCTCA GGCGTTGGCT CTCATGGAGG 2400
TGGCCTGAGG CATCTGACTC TTTCCCCTCA AGGAGTCTCT GAGTCTCCCG GAGTCAGCGC 2460
CGGCTGTTGT GGCTTTTCCC CGGGTGATAA CTGAGCCGAA TTTCCGCGCC CGCTTCAGTG 2520
GCTGCTTAGA CAGGAAGCTC CACCCAGCCG GGCGTCCTCG GCCTTCTGTG CCTCTCGGGA 2580
GGGTCCGCAT GATTCCGGAA GGGGCTCTGC TGCAGCTAGG ATGGCACCCG CCCCTGCCAG 2640
GCATAGGCAC AGCACCCTGC GGTCAGGGCC TCCGCCAGAC GTCATCAACA CTCACTTCCC 2700
CTCGAAAGCC GCCACATAGA GGGGGTATTT TCAGTGTCTT TTTTCCTGAA CAGCTATTTT 2760
AGTGTCTCTG AAAAAAACCA TCCACAGCCG TGAGCCTTCA GGGGCTGCCT GCCCTGCGTC 2820
CCCGGCCCTG TGCGCCCGAG CACTTATCTT TCTCCCTTGG GCCCAGGTCA GAGCCAGGCA 2880
CCTGCCCCTC CCCTGGCCCC ACCCTGCTTG TTCCCTGAGG GCTGCAGGGT GGGTGCACGT 2940
GCTGCAGGGG AGGCCACGGG CTTTGGCCAG ATCTTCCCCC AGGGCCCTCC ATCCCCATAA 3000
TTGGAGCACC TTGATGGACA GCCTGCCCTG CGCCCCATCT TCCCCCTAGG GAAGCAGGGT 3060
CCCTGCTGCC TCCAGGAGGC TGGTTCCTGA TGCAGCGTCT TCTCCTAGAG TCCTGGAGGT 3120
GGGAAGAGCC CCCGGCCCTG AGTGTGCTCT GTCCACCAAG GCTTCCTGGC TGAGGGCAAG 3180
GGCGGAGCCC CCACCGCCCG ACTTTGCTGC CTCCTCTTGA GGTTGGCCTC GGCAGAGTGA 3240
GTGGGACCTC ACCCCTGTGA AGGGCCCCTT GCCCTGTGTG GCCTGTTCTG CATTGGCCTG 3300
TGGTGTAGAC CTGGTGCCAG CTGCCCTGGA GACTCTGTGC TGTCCTGTGG GGTCTTTGGC 3360
AGTAGAGGAA TGGCCCATTT TACGGAGACT GCCCTGTGAT TTTGCTTGGG AAGAGACCTT 3420
GGGTCTCAGT TGTGCCTTGC GGGCAGCACC GTCTCAGGGG TTTCCAGCCG CAGGGCTGTG 3480
GGAGTTCACG TTTGCCTGAG GCTGGATGTA CCGGCTCAGG CCCCCAGCAC ACAACCCACA 3540
TCACTCACTG GCTCTTGGGG GATGTGCCTC AGCACCTGAC ACACAACACC TGGTTCTGAG 3600
TGGGCTGGGT CCAGGCACCT TCGCTAAGCT TCCTCCACCA GCGGGACCTG GTTCTGGGTG 3660
GGCTGGGTCT GGGCACCTTC GCTAAGCTTC CTCCAGCACC GGGGCTGGCA AGGAGCGAGG 3720
CAAAGGTGTG TGTGGTGCCA TCCTGTAGGA GCCAGGCTCC TTGGGGATGG TGTCCTTCAT 3780
TTTGAAAATG TTTCCTTCCC ATGGGGAGGG GGCAGCCAGA ATGCCCACTC TTTAATGCAC 3840
CTGTGCCAGT GGCCCACAGG GACACGGTGT CCCCTCCCCG CGACCACCCC TGTGCCGCAG 3900
CTGCCCTTCC CAGACGCATC CGTCGTGAGT GGCTCTCGCC GTGCTGTGGC TGGTTGAGCT 3960
GAGTGCCCAG CGCTGGGCAC CCTCTGAGGA CACACTCGGG TTCTAGGAAA GGGGTTTGGC 4020
AGGAGAAGGA CGAGGGACTC CTGGCCAGGC TGAGCCGCTG TGGAAGGGGA GAGTGGGTCT 4080
TGGTGCTCCA TCCCAAACCT GCTGCAGCCG TGGGTGAGGT CACCCGGAAT GGCAGGACAA 4140
GGTCCACTCT GTTCTCTCGG AGATGACTTG TCCCTCAGCA CAGCCTCCAC GTGCCTGTTG 4200
CGCGTGGCCT AAGGGCCTTT ATGCAAAGTG AACTTGGTCT CCTGGGGGGT GCCCTGGAAT 4260
CTGCCTTCTG CGCCACTCAG GGTCGTTTGT GGCCGGAGTG CATGGGGCTC TGACTGCCAT 4320
GTGCCAGCCA CGGGGCTGGT GGAGGGACCC TGCCCTGGGA ACCACAGGTG CCAACAAAAC 4380
CTTTCATTGA 4390
|
