| Tag | Content |
|---|
EnhancerAtlas ID | HS046-00250 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:12243870-12246770 |
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: 2 | Chromosome | Start | End |
| chr1 | 12243884 | 12246504 | | chr1 | 12245348 | 12245387 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012182 | chr1 | 12242459 | 12247879 |
|
Enhancer Sequence | CTATTCTATC TACCTATCTA TCTATCTATC TATCTATCTA CCTACCTACC TACCTACATA 60
TCTATCCATC CTCTCCGATT CCCTCACCAC TGGGTCTCAG ATTCCCTGCC TGTTAAATAA 120
ATGGTCAGTT AACCCTCAAC AGTGATTTTC AATTTTTCAC TTGAGGCCCC CATATTTTGG 180
AAGATTGTAG TTTGCTGAAC ACGCTGACTG AATCAAGTAC TATCCAACTT ATTTCCTCAT 240
TTTAACATGT CAAAGATCCC CTGTGGGGTG AGTGGGGTGT GAATTGGAGC CTCCCCAATC 300
CAAGGCACAG GAACTGGAAG CTTCTGTAGC CCTGCATTTC CTAGAGAATG CTTGCCATGT 360
TTTGGGGACC TCCTGGGGGG CCCCTGTACT GACCAGAGGC CGGCTCCCAG GGCTGTGGTT 420
TGGGCCCAGC CCCCTGCTCC TGGGGACTGC TGCTGTGGAG GGAGTGACCT TTTGTTCTGC 480
TTTGCCAAGG GGCTTTCTGT TCCTCATTGT TTAGCCATGA CAAGGCTGTG GATTTTTTTT 540
TTTTTTTCTG TCCAAGAGAA TAAACAGGCC TGAGATTGCT CAAGGGAGCC GACCCCCTCT 600
GCCAGCTACT GGGGGCTGGA GGCTCACAGA GCCAGGGAGG AAGTCCTACC CCCTCTGCCG 660
GCTACCGGGG GGGCTGGAGC CACACAGAGC CAGGGAGGAA GTCCAGGGAC GGTCACTCAC 720
AGCAAAGCCT CAGACAAGAG AGGAACCTGG AGGGGAGGAG GTGGGAGGCC ACCACTCAGC 780
CGGCCTGGGG GCCATGGGAG TCCAGCTGCC TGCCGTTAGT GGCCAGGAGC CCTCGTCCAT 840
TGCGGCTCTT GAGAGCCCAA ACTTGGCCAC GGCAGGGCTC TTTCCCATCA GGCCCTTTGA 900
GCCCTGATGG GAAACCCTTC CCCAGCCAGG GTGGGATTTC TTGCTGCCGC CTGGAGCCGC 960
CCTGGCCCTG TGGTTCTCAG GCCCTGGAGG AGTGAGGGGC TCCCCTGGTT ACCCCAAGGG 1020
CACTCGTGGG GATGAAGCCC GCGGGATGCA GGATTCCCAC GAGACCTGTG CTGGCCACTG 1080
TGCGGGGTGG GGGGCTGCCA GGGAAGAGGT GCAGCCCCTG CCTGCCTCAG GGATGCGATC 1140
TGAGGGAAGA GGCAGCTGTG TCTGGGAGGC CGTTCGGTCG GAGGGGGATA GGCACAGCCC 1200
CTGCCCTTGG GGAAGCGCCC AGCAGCAGCC TTCAGGGAAG GCAGTTTGGG GGTTTGCCGA 1260
GGGCCAGGAA GACCCTCTGC CGCAGTTAGT ATTCGATGGA ATGGCTTGTG CAGAGGGAGC 1320
TGCAGAAGCT GCCATTTCTC TGGGTTAGGG GCTCCCACAG CCTTTGGATG CCGGGTCTCG 1380
GCCATGAGCC CCCTCCGCCA CCCCTCCCCC AGGTCACCTT GCTCAATCCA GGAGGCCGGA 1440
TGATCAGAGT GTGTTCTGCA AAGGAGCGTG AGAATCACTG GGGAGATTTC CTTTTTCTTT 1500
TTCTTTCTCT TTTTTTAATG GTACAGCTTC CTGGGCCCAC CCCTGAGATT CTGCACTTGT 1560
TTGGGGAGTG GGTGTTGGCT TCATGACAGG CACCCCTGGG TGCTTTGGAC ACAGGCAGTG 1620
AGCTCCCCCC ACACTGTGTG AACCCCTGAG AAGGCTTCTC CTTTTGTCTA GGGTGCCTGG 1680
GAGTCTGCTC CAGCAGCAAA CCGGGGAGGG GAGGGGTACT GGGACCGAGT GTGTGTGGCA 1740
GCACCGTGTC CAGGCAAACT GAGGCTCCAG ACGGGGGTTA CTTCTTCAGA CCCTGTTATG 1800
CAGCATGGTT CCCACTGCCC GTGCCCAGAA TTCACCATAG CTGATGGGCC TGGGGTGGGC 1860
CTCCGGGGCA GGCCAGGGTG GAAAGTGCAT CTGTGTTTGA GCTTTGCGGC CCTGGCGCTG 1920
GAGTTAGATC CCTACAGGAA AGGACATTGT AACCCAGCCC GTGGTTGAGA CTAGCAGCTG 1980
CTGAGCACCT ACGCCCTGCT AGGCTGTGGG GCAACAGCAA AGGGTAACCC CCAGCCTGCA 2040
GCCTCAGGGG GGCTTCCCAT CTAGCGAGGG GCCCAGGGAG GCCATGAGGA GAGCCATGAG 2100
GGAGGAAGGT GGGGACTCTG GGCCTGAGTG ACTCCTTCAG GGTGGGGTGC GGGCAGGGAG 2160
CCTTCAGGAG GGAGGGTACT GCCTGAGCAG GGCTCTTAAG GGACACGTGG AATTTGTTAC 2220
AGGAAGCACC AGGCCATTCC AGGCATAGAA ATCAGCTGGG GTGCAAAGGC CTGGGGGTCA 2280
GAAGAGTGGC AGATTGCTCC ATGGCAGGAA GCCCCAGCTC CTCTGGGTCG TTCCCGCTGA 2340
GGGATTCCAG CTGTTGGCAC CGAGGGGTGC AGCCAGGGCA GGGTGGTGCT GCCTGCCAGG 2400
CTGAGGTGGG AGACAGCTGG GTTTCTAGCC CTGCTTGTCA CTCGCTATAG GTGCAGCCAA 2460
ACGCTCAGCA GGCCCAAACT CTGGGCAGTC CTGACTCCCA GGCAGTGCTG TGAGGAAGGG 2520
GAGGAGGAGG CACACTGAAC CCACCTGCTA CGTTGGCTGG TGGAAATTTG GCCAGGTCTG 2580
CACTGGCCCA GCGGTGCTGG GTGTCGTGAC TGGTGTCTGC TCTGACTGGC TTGCTGACAG 2640
CTGAAGTCCA GGATAGGTCC ATGGCCACGT TGTGCTGGTT TGTTAAATAT TTTTAGTATC 2700
TCCCCTGCTC CTATATGTTA GGTACTGGAG TCCAGAGAGG TTAAGGCACT TGCCTAAGGC 2760
CACACAGCCG CTAAGTGGTG GAGTGAGGAT TTGAAACCAG TTCTTTCTGA CTCCCTGTAT 2820
CCTTATCTAT GGAGAGGCCC CATGACTCGT TCACTAAAGG TTATGGATCT CGATCTTGTA 2880
CTGGCCACAT GACTGCAGCT 2900
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