| Tag | Content |
|---|
EnhancerAtlas ID | HS188-06350 |
Organism | Homo sapiens |
Tissue/cell | Th2 |
Coordinate | chr19:16188710-16190090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SRF | MA0083.3 | chr19:16189802-16189818 | TTACCTTATAAGGGAA | + | 6.21 | | SRF | MA0083.3 | chr19:16189802-16189818 | TTACCTTATAAGGGAA | - | 6.21 |
|
| | Number of super-enhancer constituents: 43 | ID | Coordinate | Tissue/cell |
| SE_01839 | chr19:16185787-16189800 | Aorta | | SE_01839 | chr19:16189805-16190679 | Aorta | | SE_02839 | chr19:16186206-16191437 | Astrocytes | | SE_02971 | chr19:16188692-16189720 | Bladder | | SE_02971 | chr19:16189841-16190500 | Bladder | | SE_10693 | chr19:16185790-16191508 | CD19_Primary | | SE_12394 | chr19:16185931-16191498 | CD3 | | SE_15135 | chr19:16185338-16192398 | CD4_Memory_Primary_7pool | | SE_18848 | chr19:16179215-16192677 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19514 | chr19:16185616-16192322 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22995 | chr19:16184035-16191697 | CD8_primiary | | SE_23280 | chr19:16188757-16190584 | Colon_Crypt_1 | | SE_23863 | chr19:16188827-16189637 | Colon_Crypt_2 | | SE_23863 | chr19:16189798-16190078 | Colon_Crypt_2 | | SE_24812 | chr19:16188792-16190572 | Colon_Crypt_3 | | SE_26166 | chr19:16184820-16191651 | Duodenum_Smooth_Muscle | | SE_26678 | chr19:16176293-16193132 | Esophagus | | SE_27889 | chr19:16185989-16191369 | Fetal_Intestine | | SE_28973 | chr19:16185881-16191369 | Fetal_Intestine_Large | | SE_30609 | chr19:16186003-16190851 | Fetal_Muscle | | SE_31734 | chr19:16185696-16191574 | Gastric | | SE_34724 | chr19:16185575-16191772 | HeLa | | SE_35489 | chr19:16186199-16190636 | HepG2 | | SE_36391 | chr19:16185874-16192210 | HMEC | | SE_38521 | chr19:16185905-16191769 | HUVEC | | SE_39334 | chr19:16186024-16190687 | IMR90 | | SE_42651 | chr19:16185797-16191612 | Lung | | SE_44348 | chr19:16185964-16192991 | NHDF-Ad | | SE_44969 | chr19:16186081-16191595 | NHLF | | SE_46221 | chr19:16185791-16193164 | Osteoblasts | | SE_50174 | chr19:16184776-16190644 | Sigmoid_Colon | | SE_52442 | chr19:16184771-16191534 | Small_Intestine | | SE_53411 | chr19:16176386-16192361 | Spleen | | SE_54658 | chr19:16176673-16196030 | Stomach_Smooth_Muscle | | SE_55462 | chr19:16186444-16190513 | Thymus | | SE_56641 | chr19:16186159-16191291 | u87 | | SE_57488 | chr19:16188770-16190130 | VACO_503 | | SE_58010 | chr19:16188826-16190030 | VACO_9m | | SE_59439 | chr19:16180216-16191753 | Ly3 | | SE_62472 | chr19:16180149-16231639 | Tonsil | | SE_64972 | chr19:16186350-16191416 | NHEK | | SE_66536 | chr19:16188765-16190634 | Jurkat | | SE_67443 | chr19:16186403-16191429 | MM1S |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACAGGTGCCC GCCACCACGC CCAGCTAATT TTTTTTTTTT TATTTTGGAT TTTTAGTAGA 60
GACAGTGTCT CACCATGCTG GCCAGGCTGG TCTCGAACTC CTGACCTCGT GATCTGCCCA 120
CCTTGGCCTC CCAAAGTTCT GGGATTACAA GCGTGAGCCA CGGCGCCCAG CCTCAATTGT 180
GTTTTCTCTG CCCTGGGAAG AGCTCATAGA CAAATGGAGG CAGGGGAGCT GACTCACTGA 240
TGGAGCGAGG TCTGCATTCC ACGGGTTTTC TGTGCAGTTA TGGGAGCATG ACAGGGGAGG 300
CTCCAAAATG GAGGTTGAGC TGGGTCTTAT AGAATAAATA AGTTTGCTGG GACCAGAGAC 360
ATGGGTGTGC ACAGACTCAG AGGCAAGAAA GTTGTATGAT GAGGGTGGGG GGGTGTGCGG 420
ATAGAGGTTG AAGCCCAAAA GCCCTGAAAG TTCAGTGTTG AGGCTCAGGG TGGGGACCCT 480
AGAGAGGCAA AAGATGCCCA GCCAGATGGA ATTGGTGGTG TGAATTGCCA GGACTGGAAA 540
GAGCCCAGAT GGGGGCTGCA GCATGGGCCT TGGTTGAAGC CTCTAATCCT GTAAGGGCTG 600
CTTTGGCCCA AGAGGCCTTA GAAACCCGGT GTAAGCCTCA ATCGGTAGCC GGTCTGGCCT 660
CTTTCTCACA CTTAACCGAC ACAGCTCTTG CTCTGATCTC ATCCCAAGTC ATCTCGCTGG 720
AGGACAATTA ACTCGGCTTC AAAATGGCCC TCAGCCTGGA GCCAAGATTT AGGAGCAAGA 780
CCGTCTAGTT GGGAGAGAAG ATGTTTTTGG AGAGTTGAAG ACTTCTTGAA AAAGTTCGAA 840
AAGTTCTTGA AAAAGCAAAG GATGCTTCTT TCCGTCTGGG AGAGGGAAAA CCTCTCCCAG 900
GGCAAAAGGA ACTAAGACCA GGGGTGGGTT AAAAAAAAAA AAAAAAAAAC CTTTCACTCT 960
TGTAGAATAA GCCAGGAGCC GGCGTGTGGT AGACTTCTGG GCCTGTTTCC CGACAGCTGG 1020
TTTCGTTTAG ATTTTTGTGT GATTAACTGA CATCTTCCTG TTCCTTTGCC ACATGTATCT 1080
AGCAAGCCTC TTTTACCTTA TAAGGGAAAT CCTTTGTAGC GTGTGGAAGG CTTTGATTGC 1140
AGGAAGGGGT GGAACCCAAA ATGACTCGGC CGTGACTAGC AGTTTTTCAA AAATACATAT 1200
ATATGTATGC ATGTACAGAT ATGCGTGTAT CTCCCAACTC CAGACAGCTG AAAATCTGCC 1260
AAAAGCGTTG TTTGCCAGGA TTCAGAATTT CCCACATAAG GGCTACTCAC TTCTTAAAAG 1320
ACAACTCATG AATCAAGCAC CTCTGTTTGA TCTTTAAAAT CAATTCCTCG ACTGCTAATG 1380
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