| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13101 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:37875260-37876360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr2:37875299-37875310 | TCTTATCTCTT | + | 6.02 | | Myod1 | MA0499.1 | chr2:37876043-37876056 | AGGAACAGCTGCC | - | 6.36 | | ZIC1 | MA0696.1 | chr2:37875961-37875975 | GGCCCCCTGCTGTT | + | 6.22 | | ZIC4 | MA0751.1 | chr2:37875961-37875976 | GGCCCCCTGCTGTTC | + | 6.24 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_09261 | chr2:37869712-37900786 | CD14 | | SE_10670 | chr2:37875200-37876214 | CD19_Primary | | SE_11528 | chr2:37874327-37888752 | CD20 | | SE_12153 | chr2:37874561-37876546 | CD3 | | SE_15360 | chr2:37874423-37876411 | CD4_Memory_Primary_7pool | | SE_16522 | chr2:37874293-37876198 | CD4_Naive_Primary_8pool | | SE_17964 | chr2:37869673-37877493 | CD4p_CD25-_CD45ROp_Memory | | SE_18340 | chr2:37867912-37879003 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19132 | chr2:37874200-37878226 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20286 | chr2:37869312-37879189 | CD56 | | SE_21337 | chr2:37874614-37876142 | CD8_Memory_7pool | | SE_22384 | chr2:37869116-37879185 | CD8_primiary | | SE_26476 | chr2:37874202-37875796 | Duodenum_Smooth_Muscle | | SE_32540 | chr2:37875215-37876448 | GM12878 | | SE_37038 | chr2:37871988-37888196 | HSMMtube | | SE_38334 | chr2:37870072-37887496 | HUVEC | | SE_40847 | chr2:37874429-37890176 | Left_Ventricle | | SE_42564 | chr2:37874517-37878230 | Lung | | SE_45823 | chr2:37873666-37876478 | Osteoblasts | | SE_49044 | chr2:37874593-37877111 | Right_Atrium | | SE_51815 | chr2:37874435-37878064 | Skeletal_Muscle_Myoblast | | SE_61134 | chr2:37842214-37883070 | HBL1 | | SE_62438 | chr2:37800533-37911884 | Tonsil | | SE_63609 | chr2:37874353-37878114 | HSMM | | SE_65823 | chr2:37875185-37877415 | Pancreatic_islets |
|
| | 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 |
| GH02I037633 | chr2 | 37860327 | 37886462 |
|
Enhancer Sequence | GCATTGGGGT TGTAATGTGC TCTTTTGCCA ATGAGATGCT CTTATCTCTT GAAAATAATC 60
CTCCACCTCT GATGCTGACA CAGAGAAGCT AAACCCTTTC CCACTGCAGG AACTTCCCAA 120
ATGGCTCTGC CATGACCTCT TCCCTCAGGC GCTCCTCCCA CTGGCTGCAG AGCCTGCAAA 180
TAAATACTCC AAGGGCTGGG TGGGTTAGTT GGTGTTTTGA AGGGAGCCAC ATTTGCTTGT 240
AGCAGCTGGA GGCTGTCTGC ATCTGCCCCA TATTTCTTTC CTTTCAGCAA GAGTTTTAAA 300
TTCATTTACC AGTGGCAGGT GACAAGAACT GTGCTCCACC ACCCACTGGC TCAGTAACAG 360
CTAACTCAAT TTGGGAAGCA GCTAGCTCAG CGTGTCAGCA TGCTGGCCAG CAACCCAGGC 420
CGGAGAAGGC TGAGAACAAT GCACTAGAGA GAGCCAGCCC CACTCGGGCT TTGGGTATGG 480
GGAGGAGGCA GAGAAAGTAC GAGGAGGTTT GCATTCATGC AGAGTGGGCT GACCATGGGG 540
CTGCCAGCAA TGACATGATC GTGGGTCCTG ACACTCGTTC TCATAGTTTT AGCTCTAATT 600
TGGGTCTTGT TGTGGTAACA AAAGTTGAAG CCCATGTTCT TCCTGTTAAA ACATCAGAAC 660
TTCCTTCCTG TATGAGTGTA CAATGCCTAG TCCTGGCCTC GGGCCCCCTG CTGTTCAGAG 720
GTGGCCTCCC TGCCCTTTGG GCACAGTGTG GCTGACTGCC TGCAGGAGCA GCTGGGTGGC 780
CTGAGGAACA GCTGCCCACA GGAGTGGTGT CCTCAGCACA CACGGCCAGG AAGGCAGCTG 840
CCATGGAAAG ATACAGCGTG TCCACCACAA CTCAAGGGCA TGCCAGGGCT GCCTGGGGTC 900
AGCTGATGGA GGCAGGGTTA TGCAAGGCCA GGTCCCAGGG CAGGGGGTTC CAATTATTTA 960
AAAAAAAAAA AAAAAATCGA TCACTTAAGG CCTGGAGTTT GAGGTCAGCC TGGGCAACAT 1020
AGCAAGACCC TGTCTCTATG AAAAAAAAAT TAGCTGGGCA TGGGGGCACC CGCCGGTAGT 1080
CCCAGCTACT CAGGAGGCTG 1100
|
