| Tag | Content |
|---|
EnhancerAtlas ID | HS105-00696 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:12243950-12246770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:12245361-12245382 | TTTTTCTTTTTCTTTCTCTTT | + | 6.77 | | ZNF263 | MA0528.1 | chr1:12245259-12245280 | CCCCTCCGCCACCCCTCCCCC | - | 6.22 | | ZNF263 | MA0528.1 | chr1:12246380-12246401 | TGAGGAAGGGGAGGAGGAGGC | + | 6.78 | | Znf423 | MA0116.1 | chr1:12245459-12245474 | GCACCCCTGGGTGCT | - | 6.35 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00369 | chr1:12226565-12247198 | Adipose_Nuclei | | SE_01471 | chr1:12243922-12246504 | Adrenal_Gland | | SE_04546 | chr1:12243735-12246962 | Brain_Anterior_Caudate | | SE_06521 | chr1:12243738-12246994 | Brain_Hippocampus_Middle | | SE_09154 | chr1:12224797-12249846 | CD14 | | SE_10696 | chr1:12243928-12245111 | CD19_Primary | | SE_14553 | chr1:12243811-12245422 | CD4_Memory_Primary_7pool | | SE_14553 | chr1:12245589-12247318 | CD4_Memory_Primary_7pool | | SE_17827 | chr1:12231021-12246713 | CD4p_CD25-_CD45ROp_Memory | | SE_18389 | chr1:12226183-12250288 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19117 | chr1:12243746-12249924 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20048 | chr1:12243749-12245373 | CD56 | | SE_20873 | chr1:12243794-12244892 | CD8_Memory_7pool | | SE_22347 | chr1:12243335-12245917 | CD8_primiary | | SE_26251 | chr1:12243680-12246989 | Duodenum_Smooth_Muscle | | SE_27503 | chr1:12243903-12246642 | Esophagus | | SE_30788 | chr1:12243698-12246708 | Fetal_Muscle | | SE_32030 | chr1:12243891-12246634 | Gastric | | SE_38661 | chr1:12243533-12246545 | HUVEC | | SE_41498 | chr1:12243811-12247059 | Left_Ventricle | | SE_42336 | chr1:12243813-12247305 | Lung | | SE_48967 | chr1:12243799-12246749 | Right_Atrium | | SE_50250 | chr1:12243815-12247081 | Sigmoid_Colon | | SE_52522 | chr1:12243745-12249859 | Small_Intestine | | SE_53313 | chr1:12243756-12247385 | Spleen | | SE_55394 | chr1:12243888-12244461 | Thymus | | SE_55394 | chr1:12244622-12245112 | Thymus | | SE_61096 | chr1:12184746-12245090 | HBL1 |
|
| | 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 |
| GH01I012182 | chr1 | 12242459 | 12247879 |
|
Enhancer Sequence | CCCTCACCAC TGGGTCTCAG ATTCCCTGCC TGTTAAATAA ATGGTCAGTT AACCCTCAAC 60
AGTGATTTTC AATTTTTCAC TTGAGGCCCC CATATTTTGG AAGATTGTAG TTTGCTGAAC 120
ACGCTGACTG AATCAAGTAC TATCCAACTT ATTTCCTCAT TTTAACATGT CAAAGATCCC 180
CTGTGGGGTG AGTGGGGTGT GAATTGGAGC CTCCCCAATC CAAGGCACAG GAACTGGAAG 240
CTTCTGTAGC CCTGCATTTC CTAGAGAATG CTTGCCATGT TTTGGGGACC TCCTGGGGGG 300
CCCCTGTACT GACCAGAGGC CGGCTCCCAG GGCTGTGGTT TGGGCCCAGC CCCCTGCTCC 360
TGGGGACTGC TGCTGTGGAG GGAGTGACCT TTTGTTCTGC TTTGCCAAGG GGCTTTCTGT 420
TCCTCATTGT TTAGCCATGA CAAGGCTGTG GATTTTTTTT TTTTTTTCTG TCCAAGAGAA 480
TAAACAGGCC TGAGATTGCT CAAGGGAGCC GACCCCCTCT GCCAGCTACT GGGGGCTGGA 540
GGCTCACAGA GCCAGGGAGG AAGTCCTACC CCCTCTGCCG GCTACCGGGG GGGCTGGAGC 600
CACACAGAGC CAGGGAGGAA GTCCAGGGAC GGTCACTCAC AGCAAAGCCT CAGACAAGAG 660
AGGAACCTGG AGGGGAGGAG GTGGGAGGCC ACCACTCAGC CGGCCTGGGG GCCATGGGAG 720
TCCAGCTGCC TGCCGTTAGT GGCCAGGAGC CCTCGTCCAT TGCGGCTCTT GAGAGCCCAA 780
ACTTGGCCAC GGCAGGGCTC TTTCCCATCA GGCCCTTTGA GCCCTGATGG GAAACCCTTC 840
CCCAGCCAGG GTGGGATTTC TTGCTGCCGC CTGGAGCCGC CCTGGCCCTG TGGTTCTCAG 900
GCCCTGGAGG AGTGAGGGGC TCCCCTGGTT ACCCCAAGGG CACTCGTGGG GATGAAGCCC 960
GCGGGATGCA GGATTCCCAC GAGACCTGTG CTGGCCACTG TGCGGGGTGG GGGGCTGCCA 1020
GGGAAGAGGT GCAGCCCCTG CCTGCCTCAG GGATGCGATC TGAGGGAAGA GGCAGCTGTG 1080
TCTGGGAGGC CGTTCGGTCG GAGGGGGATA GGCACAGCCC CTGCCCTTGG GGAAGCGCCC 1140
AGCAGCAGCC TTCAGGGAAG GCAGTTTGGG GGTTTGCCGA GGGCCAGGAA GACCCTCTGC 1200
CGCAGTTAGT ATTCGATGGA ATGGCTTGTG CAGAGGGAGC TGCAGAAGCT GCCATTTCTC 1260
TGGGTTAGGG GCTCCCACAG CCTTTGGATG CCGGGTCTCG GCCATGAGCC CCCTCCGCCA 1320
CCCCTCCCCC AGGTCACCTT GCTCAATCCA GGAGGCCGGA TGATCAGAGT GTGTTCTGCA 1380
AAGGAGCGTG AGAATCACTG GGGAGATTTC CTTTTTCTTT TTCTTTCTCT TTTTTTAATG 1440
GTACAGCTTC CTGGGCCCAC CCCTGAGATT CTGCACTTGT TTGGGGAGTG GGTGTTGGCT 1500
TCATGACAGG CACCCCTGGG TGCTTTGGAC ACAGGCAGTG AGCTCCCCCC ACACTGTGTG 1560
AACCCCTGAG AAGGCTTCTC CTTTTGTCTA GGGTGCCTGG GAGTCTGCTC CAGCAGCAAA 1620
CCGGGGAGGG GAGGGGTACT GGGACCGAGT GTGTGTGGCA GCACCGTGTC CAGGCAAACT 1680
GAGGCTCCAG ACGGGGGTTA CTTCTTCAGA CCCTGTTATG CAGCATGGTT CCCACTGCCC 1740
GTGCCCAGAA TTCACCATAG CTGATGGGCC TGGGGTGGGC CTCCGGGGCA GGCCAGGGTG 1800
GAAAGTGCAT CTGTGTTTGA GCTTTGCGGC CCTGGCGCTG GAGTTAGATC CCTACAGGAA 1860
AGGACATTGT AACCCAGCCC GTGGTTGAGA CTAGCAGCTG CTGAGCACCT ACGCCCTGCT 1920
AGGCTGTGGG GCAACAGCAA AGGGTAACCC CCAGCCTGCA GCCTCAGGGG GGCTTCCCAT 1980
CTAGCGAGGG GCCCAGGGAG GCCATGAGGA GAGCCATGAG GGAGGAAGGT GGGGACTCTG 2040
GGCCTGAGTG ACTCCTTCAG GGTGGGGTGC GGGCAGGGAG CCTTCAGGAG GGAGGGTACT 2100
GCCTGAGCAG GGCTCTTAAG GGACACGTGG AATTTGTTAC AGGAAGCACC AGGCCATTCC 2160
AGGCATAGAA ATCAGCTGGG GTGCAAAGGC CTGGGGGTCA GAAGAGTGGC AGATTGCTCC 2220
ATGGCAGGAA GCCCCAGCTC CTCTGGGTCG TTCCCGCTGA GGGATTCCAG CTGTTGGCAC 2280
CGAGGGGTGC AGCCAGGGCA GGGTGGTGCT GCCTGCCAGG CTGAGGTGGG AGACAGCTGG 2340
GTTTCTAGCC CTGCTTGTCA CTCGCTATAG GTGCAGCCAA ACGCTCAGCA GGCCCAAACT 2400
CTGGGCAGTC CTGACTCCCA GGCAGTGCTG TGAGGAAGGG GAGGAGGAGG CACACTGAAC 2460
CCACCTGCTA CGTTGGCTGG TGGAAATTTG GCCAGGTCTG CACTGGCCCA GCGGTGCTGG 2520
GTGTCGTGAC TGGTGTCTGC TCTGACTGGC TTGCTGACAG CTGAAGTCCA GGATAGGTCC 2580
ATGGCCACGT TGTGCTGGTT TGTTAAATAT TTTTAGTATC TCCCCTGCTC CTATATGTTA 2640
GGTACTGGAG TCCAGAGAGG TTAAGGCACT TGCCTAAGGC CACACAGCCG CTAAGTGGTG 2700
GAGTGAGGAT TTGAAACCAG TTCTTTCTGA CTCCCTGTAT CCTTATCTAT GGAGAGGCCC 2760
CATGACTCGT TCACTAAAGG TTATGGATCT CGATCTTGTA CTGGCCACAT GACTGCAGCT 2820
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