| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11320 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:39168670-39171590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr19:39171401-39171422 | CCCTCACCTTCCTCCTTCTCT | - | 6.4 |
|
| | Number of super-enhancer constituents: 63 | ID | Coordinate | Tissue/cell |
| SE_00117 | chr19:39168564-39169764 | Adipose_Nuclei | | SE_00865 | chr19:39168890-39170449 | Adrenal_Gland | | SE_00865 | chr19:39170550-39171587 | Adrenal_Gland | | SE_01543 | chr19:39164445-39171596 | Aorta | | SE_04868 | chr19:39168734-39169885 | Brain_Cingulate_Gyrus | | SE_05805 | chr19:39164448-39170203 | Brain_Hippocampus_Middle | | SE_07777 | chr19:39168707-39170257 | Brain_Inferior_Temporal_Lobe | | SE_09404 | chr19:39164511-39180526 | CD14 | | SE_13490 | chr19:39168489-39169894 | CD34_Primary_RO01536 | | SE_14624 | chr19:39168532-39170061 | CD4_Memory_Primary_7pool | | SE_14624 | chr19:39170904-39172653 | CD4_Memory_Primary_7pool | | SE_19537 | chr19:39170346-39172578 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20249 | chr19:39164561-39178319 | CD56 | | SE_20865 | chr19:39164617-39170179 | CD8_Memory_7pool | | SE_20865 | chr19:39170480-39179166 | CD8_Memory_7pool | | SE_22709 | chr19:39168508-39169910 | CD8_primiary | | SE_22709 | chr19:39169957-39177919 | CD8_primiary | | SE_23062 | chr19:39168629-39171558 | Colon_Crypt_1 | | SE_23732 | chr19:39168972-39169508 | Colon_Crypt_2 | | SE_23732 | chr19:39169641-39170175 | Colon_Crypt_2 | | SE_23732 | chr19:39170522-39170855 | Colon_Crypt_2 | | SE_23732 | chr19:39170961-39171539 | Colon_Crypt_2 | | SE_24739 | chr19:39168930-39170258 | Colon_Crypt_3 | | SE_24739 | chr19:39170416-39170866 | Colon_Crypt_3 | | SE_24739 | chr19:39170896-39171572 | Colon_Crypt_3 | | SE_25779 | chr19:39164448-39177989 | Duodenum_Smooth_Muscle | | SE_26525 | chr19:39168562-39171587 | Esophagus | | SE_27614 | chr19:39164407-39180553 | Fetal_Intestine | | SE_28533 | chr19:39164445-39201888 | Fetal_Intestine_Large | | SE_31384 | chr19:39168565-39170223 | Gastric | | SE_31384 | chr19:39170454-39171474 | Gastric | | SE_34299 | chr19:39169159-39170485 | HCT-116 | | SE_34681 | chr19:39168850-39169639 | HeLa | | SE_34681 | chr19:39170836-39180506 | HeLa | | SE_35812 | chr19:39168616-39191950 | HMEC | | SE_36926 | chr19:39168763-39172804 | HSMMtube | | SE_38012 | chr19:39168814-39172845 | HUVEC | | SE_40018 | chr19:39168791-39169939 | K562 | | SE_40018 | chr19:39171034-39171644 | K562 | | SE_40594 | chr19:39164568-39178326 | Left_Ventricle | | SE_41601 | chr19:39169253-39169628 | LNCaP | | SE_42097 | chr19:39164441-39171613 | Lung | | SE_45660 | chr19:39168564-39172655 | Osteoblasts | | SE_47114 | chr19:39164477-39226374 | Panc1 | | SE_47461 | chr19:39168979-39170222 | Pancreas | | SE_47461 | chr19:39170953-39171437 | Pancreas | | SE_48075 | chr19:39168529-39178289 | Psoas_Muscle | | SE_48555 | chr19:39168554-39171607 | Right_Atrium | | SE_49449 | chr19:39168880-39169517 | Right_Ventricle | | SE_49449 | chr19:39170918-39171396 | Right_Ventricle | | SE_50056 | chr19:39164598-39172640 | Sigmoid_Colon | | SE_51136 | chr19:39168650-39169947 | Skeletal_Muscle | | SE_51136 | chr19:39170726-39172632 | Skeletal_Muscle | | SE_51705 | chr19:39169468-39170771 | Skeletal_Muscle_Myoblast | | SE_51705 | chr19:39170881-39171625 | Skeletal_Muscle_Myoblast | | SE_52339 | chr19:39168564-39178308 | Small_Intestine | | SE_53291 | chr19:39168797-39169709 | Spleen | | SE_53291 | chr19:39169852-39171576 | Spleen | | SE_55638 | chr19:39170884-39171285 | Thymus | | SE_56725 | chr19:39168926-39171553 | VACO_400 | | SE_62811 | chr19:39125155-39186863 | Tonsil | | SE_63494 | chr19:39169454-39171639 | HSMM | | SE_65266 | chr19:39168886-39178027 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 39171030 | 39171442 | | chr19 | 39169518 | 39170091 | | chr19 | 39170251 | 39170884 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I038673 | chr19 | 39164536 | 39206516 |
|
Enhancer Sequence | AGGATGCTTT GCAAGTAGGC AGAAGAGGGA GACATCACTG TCCCATGGAG AGGTGGGAAA 60
ATCATCGTTA GCACAGGATA ATTCATCCTA TTTTGTGCTC ATGTTTACTG AGCTAGGATT 120
GACCTGTGTC CGGGCAGCAG GGACACAGAG GTGAGTAAGA CAAAGAGAAG GCCCTTGCCC 180
TTAAAAATGA TACGTGTGGC TAAAACGCTG TAGACCTTTT TGTTTTTTCC TTTTTGAGAC 240
TTCCTTTTTA TACAGAAATT GCTACCTGCA GGTAAAATTA ACTTACATCG TGAAAGCGAC 300
AGTAAAGTGT TTCTAGGGAT AGCTAAAGAC CTAAGAACAC AGCCCTGTGG TTTGACTGGC 360
TGGCCACCTT CCTGCAGCTG GGTTTACTAT GGTGCTGTGT TCTGGGACAG CCCACTCGTC 420
TCCATTTATT GGGCTGAGCC TCGAGACCTG CAATACCAGG GAAGGAAGGG AAGTCTAGGC 480
TGTCTTTGGT GGCCATTGTT ATTTATGGGG CATCGGCAGA GAAGTCAGTA CCATGGAAAA 540
TCTAGAGAAA GATAGAGGAT ACGCAGTGTG GTTGAGCAGA ATCTGATAGC TCCCTGGCTC 600
TCTCCGGGCC ATGGGACCCA GGGCGACACA GCCACCCTTT TTCTCTCTGC TGTCTGGCTT 660
GGGCTTGGGC TTTGTCTCCT GTGTCCCTCC ACACCTTCTT CGCTGTCAGT GGTGACCAAT 720
CCCGTGGAAT CAGCCACTGT GTGTTACCCC AAGTCCTTGC CCCTGGGACC TCGCTCTGTT 780
CGGAGACAAA ACCCGGGACT GTTTCTCCTT TTAAATGCAA CCTTGTTCCA CAGGAGAGGA 840
GAAAAGCAAG AAAGAGGTGG CTTGTTTATC TGATGGTAGT GGGGTGTGCT CTGATATGCC 900
TTTGAAAGGG GCCCAGCTTT GCTTTGCCCA GCGGCCTTTG CAGGATAATG AGAGAAGGAA 960
AACACAGGGA ACTTAGTGGG AATTTGAAAC TGGAGTGTGG GAGTGGGAAA GTTCAGCTTT 1020
TACCTTGGAG CAATCCAGTC TTTCTCCTGT AGGAAAACAG AATGGTGCTG TATGGCCTCC 1080
AAGCTGGGTT ACATCCTGGG AAAAAGACAC GTGCTTGGCT ATTGGCCTGG GCGCAGTTTA 1140
TGTGTAAGCC TTTCCTTGTG GATTCCATTT TCTTATTTCC CGAATACTTC TCAGCCCCAC 1200
AAGTCCACTG AGTCTTCTGT CTCCAGAGAC TGCCTGGTTT CCATCCCCGA GGGCATCTGC 1260
GCATCACTTA CCATGGTGTA CCATGCACCT CCAGTGTGCC CGGCACTGTG TCAGGAGCTG 1320
GGGATACAGG TGCTGGTCCC CACCTCACTC CCCTCAACCT CTGCAATATA TGATACATAA 1380
CCCACACACA CAGACCATAT GCAAAAGTGG TGGGACTCCT TTGTACCTGT CACCTGCATC 1440
AGTGATTATC AGCATTTTGC CAGACTTGTT TCATCAGTGT CTCCCAACAC ACTCCCCCCA 1500
GACATTACCC ATACGTGCTC AAATAGATTT GGGTGTGCGT GTGTGTGTGT GTGTGTGTGT 1560
GTGTGTGTGT ATTTTTTTAG AGACAGGGTC TCGCCCTGTC ACCCAGGCTG GAGTACAGTG 1620
GTGAGATCAT AGCTCACTGC GGCCTCTGAA CTCCTGGGCT TGCTTTGTTG CCCAGGCTGG 1680
TCTCAGAACT CCTGGCCTCA AGCGATTCTG CCACCTTAGC CTCCCAAAAT GCTGGGATTA 1740
CAAGTGTGAG CCACCGCACC CGGCCAATGT ATGTATTTTT AAACATAACC ACATACTGTT 1800
ATATTTAATG CTTCTGACCA TGTCTTAAGA AAAAAACAAA AACTCCCTTT GGCTTCCTTG 1860
ACATCACAGT CTCTCTGTTT CTCTGACTCT TCTTCCTCAT CTCCTATGGC TAAATTCTCT 1920
CCCTCTGTCC ACTGCTTACA CATGGGCATT TCACAATGTC CTTTTTCCCT GAAGGAACTT 1980
ACCCCCTCCC CTCAGCCTTA AGTACCCCAT CTGTGGGGAT GATGCCCATG CCTGTAGTCC 2040
TGACTCACTC ACCACGCTCT ATCGCAGTTA TTTACTGATG CATCTCTCTC CCCTATCAGA 2100
CGCTGAGGTC TTTGATGGAG CAACCTTGTA TTTGTCCGTG TATCCCCAGC ACCACACCTG 2160
TCCATAGCTG GAGCTCAGGA AGTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTAAAGT 2220
CAGAGTCTCA CTCAGTCGCC CAGGCTAGAG TGCAGTGGCA CAATCTTGGC TCACTGCAAC 2280
CTCCACCTCC TGGGTTCAAG CAAGCACGTC TGGGTAATTT TTGTATTTTT AGTAGAGATG 2340
GGGTTTCACC ATTTGGCCAG GCTGGTCTCG AAGTCCTGAC TGCAAGTGAT CTGGCCGCCT 2400
TTGGCTCCCA GATTGCTGGG ATTACAGACA GGCATGAGCC ACTGCGCCCG GCCTCAGGAA 2460
GTAGTTGAAT GAGTGACTGA ATGAATGCCC ACGTGAGCAA ATGACCTGTT TGCTGAACTT 2520
TAGACTGACG TTGCCTGATG CCCACTGCTT GTGCAGTACG TACTTCAGTC TCAGCGTGTC 2580
TGAGACCAAA CTCATTTTCA AGTCCCACTT CTTGGGCTTG GCATTGCCCA TTTGTCAGCC 2640
ATCCGAGTCA GAAACCTTGG AGTCAGCTTT TGACTTCTCA TCCTGTAACA GGCACCAAGT 2700
TTGATTTCTT TCCCTTGAAT ATCTCTTAGA ACCCTCACCT TCCTCCTTCT CTTTATTCCT 2760
ACCATTGTCC TTACTCAGGA CCATATAGTG AGGGTTTAAA AGTGCAGAGT CTTGGCCGGG 2820
TGCGGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGCGGGT AGATCACCTG 2880
AGGTCAGGAG TTCGAGACCA GCCTGGCCAA CATGGTGAAA 2920
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