Tag | Content |
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EnhancerAtlas ID | HS052-00285 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:12212830-12214400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:12213290-12213301 | TGTGACTCATC | + | 6.14 | JUND | MA0491.1 | chr1:12213290-12213301 | TGTGACTCATC | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr1:12214116-12214131 | AAGGTCAGGAGTTCA | + | 6.04 | SPIC | MA0687.1 | chr1:12213408-12213422 | TTCTTCCTCTTTTG | - | 6.62 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00369 | chr1:12212169-12214461 | Adipose_Nuclei | SE_01471 | chr1:12212830-12213765 | Adrenal_Gland | SE_09154 | chr1:12199965-12214486 | CD14 | SE_10696 | chr1:12207898-12214373 | CD19_Primary | SE_11902 | chr1:12208865-12214231 | CD3 | SE_14553 | chr1:12208809-12214332 | CD4_Memory_Primary_7pool | SE_15480 | chr1:12208768-12214030 | CD4_Memory_Primary_8pool | SE_16369 | chr1:12212506-12213878 | CD4_Naive_Primary_8pool | SE_16946 | chr1:12210087-12214122 | CD4p_CD225int_CD127p_Tmem | SE_17650 | chr1:12208923-12214185 | CD4p_CD25-_CD45RAp_Naive | SE_17827 | chr1:12206501-12214454 | CD4p_CD25-_CD45ROp_Memory | SE_18389 | chr1:12206868-12214379 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19117 | chr1:12208827-12214340 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20048 | chr1:12207907-12214477 | CD56 | SE_20873 | chr1:12208284-12214108 | CD8_Memory_7pool | SE_22347 | chr1:12207903-12214404 | CD8_primiary | SE_26251 | chr1:12206411-12213727 | Duodenum_Smooth_Muscle | SE_27503 | chr1:12212703-12214088 | Esophagus | SE_30788 | chr1:12212889-12214071 | Fetal_Muscle | SE_32030 | chr1:12212751-12214118 | Gastric | SE_38661 | chr1:12212782-12214329 | HUVEC | SE_41498 | chr1:12212621-12214203 | Left_Ventricle | SE_42336 | chr1:12209781-12214078 | Lung | SE_48967 | chr1:12212801-12214137 | Right_Atrium | SE_50250 | chr1:12207958-12214180 | Sigmoid_Colon | SE_52522 | chr1:12206320-12214007 | Small_Intestine | SE_53313 | chr1:12206186-12214442 | Spleen | SE_55394 | chr1:12212891-12213422 | Thymus | SE_59216 | chr1:12197780-12224862 | Ly3 | SE_61096 | chr1:12184746-12245090 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I012140 | chr1 | 12200161 | 12214656 |
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Enhancer Sequence | AGACTTGAAC CCAGGTCTAG GTGATGGCAA AGTTGATGCT ATTTCTCCTT TTGATATACC 60 CCAACTGTCT AAAGCAGCCC TTTTTTTTGC TAGGCTTCTT GGTGTTTGAA AATTTACCAC 120 TCATTCCTAG GAGCTAAAGG TTCCTGGGTT CCTCCTTGGG GCACATGTCT AGGAGCAGGA 180 TCTCGATCTG GTGGCAGAGG GGCAGCAGCT GCTCCGTCTG GCATACAGTA GGTGCTCAGT 240 AAGTCTGCGG GGCAGGCAGG ACAAGCCTGG GTTGGAAGGA GGTCCAGTTT CTTGGGAGTG 300 AGAGCCTCAA GACCAACTTC ACCTGAAGGA CAAATGAGAG GTGGCCGAAT CACTGCCAGC 360 TACTTCAAGA AGCCCCTAGG ACACTCCAGC CAAGGTGCCT TGGTCCCTTT TCTAAGTCGC 420 CTGCCCACCC TGCCCAAGCT CCTGCGGGGA GTGTGCCCAC TGTGACTCAT CCACGCCCAG 480 CCCTGCCCAG CTCTCACTGG GGCAGCAGTA GGCACACATA CTCGTAAAAG TCTGAATAAG 540 TGAAGACTGG GAAATTGCAC CAGGGAAAAA CTACTTATTT CTTCCTCTTT TGAATTGGGG 600 AGGGGAAATG TTGCGGGGGA AATGAGGTCA GTGACGTGGT GAGCATTTCA TGCTCCTTAC 660 TGATGAGCAG AGGGCCGGTA TCACGTGCTG CCTTCCTAGG GAGGGCTGGG TAGTGCGTCA 720 AGGAAATGGG CCCAGAGCTG TGTCTCGTCC AGTCTAGCAG GAAACTGCCC ATCTCACTGT 780 GTCACTCCCT TCTCTGTCCT TGCTCTAAGC CTCTACCCTG ACTGCCCTTG CTCTGAGCTG 840 AAATCTCACT AATGAGAAAA AAATGTGCTG GTTTATGCCT CTGTGGGCTG GCTGGGCTGG 900 TAGGTCCCAG GGGGCAGCAT GGCCTGGAGG AAACCGAGTG CACGGGGCAA GGATGATGTG 960 CACGAGTGGT ATGTGACTCC CAGGGCTCAC AGCCTCATGC AGCCCCTCCC TCTGAGAGTA 1020 TAGATGGGGA AACTGAGGCC TGAGAAGGCG AGAGATGTGC CTGAGGTCAC ACAGAGAATC 1080 CGTGGCCCTC AGCACAAGCA CCCAGTTTGC TGGTACTTTA AAGATAAAAA TAAACAAACT 1140 TTATAAATGG AAAAGATGAA TAAAAGAAGA AACGAAGTAT AAGGAATATG ATAAATATAA 1200 TAAAAATTAC ACACAATCTT GGCGAGGCAC AGTGGCTCAT GCTAGTAATC CTAACACTTT 1260 GGGAGGCCCA GATGGGCAGA TCATTTAAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT 1320 GGTGAAACCC CATCTCTACT AAAAATACAA AAATTAGTTG GGCATGGTGG TGCGCGCCTG 1380 TGGTCCCAGC TACTTGGGAG GCTGAGGCAC GAGAATCACT TGAACCCAGC AGGCGGAGTT 1440 TGCAGCAAGC TGAGATCACG CCACTGCACT CCAGCCTGGG TGATGCAGCC AGACCAAGAC 1500 CTTGTAACAA CAACAACAAA AGTAAAACAA TCAGTATTCC TTAAAAAAAA AAAAAATTGC 1560 ACACAATCCC 1570
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