| Tag | Content |
|---|
EnhancerAtlas ID | HS116-00337 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr1:12243920-12246770 |
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 | TACCTACATA TCTATCCATC CTCTCCGATT CCCTCACCAC TGGGTCTCAG ATTCCCTGCC 60
TGTTAAATAA ATGGTCAGTT AACCCTCAAC AGTGATTTTC AATTTTTCAC TTGAGGCCCC 120
CATATTTTGG AAGATTGTAG TTTGCTGAAC ACGCTGACTG AATCAAGTAC TATCCAACTT 180
ATTTCCTCAT TTTAACATGT CAAAGATCCC CTGTGGGGTG AGTGGGGTGT GAATTGGAGC 240
CTCCCCAATC CAAGGCACAG GAACTGGAAG CTTCTGTAGC CCTGCATTTC CTAGAGAATG 300
CTTGCCATGT TTTGGGGACC TCCTGGGGGG CCCCTGTACT GACCAGAGGC CGGCTCCCAG 360
GGCTGTGGTT TGGGCCCAGC CCCCTGCTCC TGGGGACTGC TGCTGTGGAG GGAGTGACCT 420
TTTGTTCTGC TTTGCCAAGG GGCTTTCTGT TCCTCATTGT TTAGCCATGA CAAGGCTGTG 480
GATTTTTTTT TTTTTTTCTG TCCAAGAGAA TAAACAGGCC TGAGATTGCT CAAGGGAGCC 540
GACCCCCTCT GCCAGCTACT GGGGGCTGGA GGCTCACAGA GCCAGGGAGG AAGTCCTACC 600
CCCTCTGCCG GCTACCGGGG GGGCTGGAGC CACACAGAGC CAGGGAGGAA GTCCAGGGAC 660
GGTCACTCAC AGCAAAGCCT CAGACAAGAG AGGAACCTGG AGGGGAGGAG GTGGGAGGCC 720
ACCACTCAGC CGGCCTGGGG GCCATGGGAG TCCAGCTGCC TGCCGTTAGT GGCCAGGAGC 780
CCTCGTCCAT TGCGGCTCTT GAGAGCCCAA ACTTGGCCAC GGCAGGGCTC TTTCCCATCA 840
GGCCCTTTGA GCCCTGATGG GAAACCCTTC CCCAGCCAGG GTGGGATTTC TTGCTGCCGC 900
CTGGAGCCGC CCTGGCCCTG TGGTTCTCAG GCCCTGGAGG AGTGAGGGGC TCCCCTGGTT 960
ACCCCAAGGG CACTCGTGGG GATGAAGCCC GCGGGATGCA GGATTCCCAC GAGACCTGTG 1020
CTGGCCACTG TGCGGGGTGG GGGGCTGCCA GGGAAGAGGT GCAGCCCCTG CCTGCCTCAG 1080
GGATGCGATC TGAGGGAAGA GGCAGCTGTG TCTGGGAGGC CGTTCGGTCG GAGGGGGATA 1140
GGCACAGCCC CTGCCCTTGG GGAAGCGCCC AGCAGCAGCC TTCAGGGAAG GCAGTTTGGG 1200
GGTTTGCCGA GGGCCAGGAA GACCCTCTGC CGCAGTTAGT ATTCGATGGA ATGGCTTGTG 1260
CAGAGGGAGC TGCAGAAGCT GCCATTTCTC TGGGTTAGGG GCTCCCACAG CCTTTGGATG 1320
CCGGGTCTCG GCCATGAGCC CCCTCCGCCA CCCCTCCCCC AGGTCACCTT GCTCAATCCA 1380
GGAGGCCGGA TGATCAGAGT GTGTTCTGCA AAGGAGCGTG AGAATCACTG GGGAGATTTC 1440
CTTTTTCTTT TTCTTTCTCT TTTTTTAATG GTACAGCTTC CTGGGCCCAC CCCTGAGATT 1500
CTGCACTTGT TTGGGGAGTG GGTGTTGGCT TCATGACAGG CACCCCTGGG TGCTTTGGAC 1560
ACAGGCAGTG AGCTCCCCCC ACACTGTGTG AACCCCTGAG AAGGCTTCTC CTTTTGTCTA 1620
GGGTGCCTGG GAGTCTGCTC CAGCAGCAAA CCGGGGAGGG GAGGGGTACT GGGACCGAGT 1680
GTGTGTGGCA GCACCGTGTC CAGGCAAACT GAGGCTCCAG ACGGGGGTTA CTTCTTCAGA 1740
CCCTGTTATG CAGCATGGTT CCCACTGCCC GTGCCCAGAA TTCACCATAG CTGATGGGCC 1800
TGGGGTGGGC CTCCGGGGCA GGCCAGGGTG GAAAGTGCAT CTGTGTTTGA GCTTTGCGGC 1860
CCTGGCGCTG GAGTTAGATC CCTACAGGAA AGGACATTGT AACCCAGCCC GTGGTTGAGA 1920
CTAGCAGCTG CTGAGCACCT ACGCCCTGCT AGGCTGTGGG GCAACAGCAA AGGGTAACCC 1980
CCAGCCTGCA GCCTCAGGGG GGCTTCCCAT CTAGCGAGGG GCCCAGGGAG GCCATGAGGA 2040
GAGCCATGAG GGAGGAAGGT GGGGACTCTG GGCCTGAGTG ACTCCTTCAG GGTGGGGTGC 2100
GGGCAGGGAG CCTTCAGGAG GGAGGGTACT GCCTGAGCAG GGCTCTTAAG GGACACGTGG 2160
AATTTGTTAC AGGAAGCACC AGGCCATTCC AGGCATAGAA ATCAGCTGGG GTGCAAAGGC 2220
CTGGGGGTCA GAAGAGTGGC AGATTGCTCC ATGGCAGGAA GCCCCAGCTC CTCTGGGTCG 2280
TTCCCGCTGA GGGATTCCAG CTGTTGGCAC CGAGGGGTGC AGCCAGGGCA GGGTGGTGCT 2340
GCCTGCCAGG CTGAGGTGGG AGACAGCTGG GTTTCTAGCC CTGCTTGTCA CTCGCTATAG 2400
GTGCAGCCAA ACGCTCAGCA GGCCCAAACT CTGGGCAGTC CTGACTCCCA GGCAGTGCTG 2460
TGAGGAAGGG GAGGAGGAGG CACACTGAAC CCACCTGCTA CGTTGGCTGG TGGAAATTTG 2520
GCCAGGTCTG CACTGGCCCA GCGGTGCTGG GTGTCGTGAC TGGTGTCTGC TCTGACTGGC 2580
TTGCTGACAG CTGAAGTCCA GGATAGGTCC ATGGCCACGT TGTGCTGGTT TGTTAAATAT 2640
TTTTAGTATC TCCCCTGCTC CTATATGTTA GGTACTGGAG TCCAGAGAGG TTAAGGCACT 2700
TGCCTAAGGC CACACAGCCG CTAAGTGGTG GAGTGAGGAT TTGAAACCAG TTCTTTCTGA 2760
CTCCCTGTAT CCTTATCTAT GGAGAGGCCC CATGACTCGT TCACTAAAGG TTATGGATCT 2820
CGATCTTGTA CTGGCCACAT GACTGCAGCT 2850
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