| Tag | Content |
|---|
EnhancerAtlas ID | HS149-00745 |
Organism | Homo sapiens |
Tissue/cell | NKC |
Coordinate | chr2:235370600-235373470 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:235372690-235372711 | ACTTGCTTTCTCTTTCCCCTT | + | 6.85 | | Klf1 | MA0493.1 | chr2:235371076-235371087 | TGGGTGTGGCC | - | 6.62 | | RUNX1 | MA0002.2 | chr2:235372844-235372855 | CTCTGTGGTTT | + | 6.14 | | ZEB1 | MA0103.3 | chr2:235372749-235372760 | GCGCAGGTGGG | - | 6.62 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_12138 | chr2:235370493-235374385 | CD3 | | SE_15186 | chr2:235371019-235374938 | CD4_Memory_Primary_7pool | | SE_15717 | chr2:235371537-235374169 | CD4_Memory_Primary_8pool | | SE_15855 | chr2:235371599-235374628 | CD4_Naive_Primary_7pool | | SE_16669 | chr2:235371235-235374243 | CD4_Naive_Primary_8pool | | SE_17253 | chr2:235371218-235374369 | CD4p_CD225int_CD127p_Tmem | | SE_17340 | chr2:235370369-235375247 | CD4p_CD25-_CD45RAp_Naive | | SE_18338 | chr2:235370557-235375206 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19377 | chr2:235371809-235374223 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20680 | chr2:235371800-235373598 | CD56 | | SE_21778 | chr2:235372033-235373957 | CD8_Naive_7pool | | SE_21942 | chr2:235371065-235374145 | CD8_Naive_8pool | | SE_22492 | chr2:235370764-235373991 | CD8_primiary | | SE_25346 | chr2:235366664-235377811 | DND41 | | SE_30954 | chr2:235371425-235374891 | Fetal_Thymus | | SE_39425 | chr2:235371200-235371898 | Jurkat | | SE_39425 | chr2:235371971-235374013 | Jurkat | | SE_50007 | chr2:235372122-235373223 | RPMI-8402 | | SE_55130 | chr2:235371389-235371907 | Thymus | | SE_55130 | chr2:235371954-235375082 | Thymus | | SE_62784 | chr2:235328691-235374533 | Tonsil | | SE_66333 | chr2:235371200-235371898 | Jurkat | | SE_66333 | chr2:235371971-235374013 | Jurkat |
|
| | 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 |
| GH02I234461 | chr2 | 235370631 | 235374948 |
|
Enhancer Sequence | CTGAGCACAG CCCAGGACTG CGTCTGGGAG AGCACCAGTT GAATTGTTCA CCCCCGAAAC 60
AACACAGGAG GACATTCATT GGTCAGGCTC ATGCAAGTTT CCAATCTGCT TGACTGGTAT 120
GGCTCTTCCT ACAAACCAGC TCATCGGCAT TATAGTCTTG ATCAGTTCTT GTCCCTAAAA 180
CGACAGAGTT CCTGAGCCTT CAGGGAAGAG GGTCACATTC TTGACCCCAA TTGCTTCCCC 240
AGGTAGGGCC CAGCCTGGCT ACCAGCCGGC TTCTCCAGGC AGCACATTGC ACACTCTGGA 300
GCAAGTCGGC CCCCAAACTC AACCAGTCAT CTTCATGGAT ATGCCGTTGG CCGACAAACC 360
CACGTCCCCA CCTCATCTCC AAAGTTCTGA TGATTGCAAC ATTCACACTT TCACTCAACC 420
TTACCACTTT GGGCTGTGAT CCTCTTAGGG CCACAGTAGG TGAAATCTTA GCCAGATGGG 480
TGTGGCCTCA CAGCAAGACT TGGCTACAGC CCCTGTGGCT GCATCCGTCC TTATGAGTGA 540
ACTCTTTCCA CAGATCATAG GAGCATGTTT CTCCCACTTC AGTCAGCAGC TTTCCCCTGG 600
ACAGCCTTCC AGGCTTCCAC TACTGCCCCC CTACCCCACT GCCCAGGGTT CAATAGTTGC 660
CATTTCCAAC TGGTCCTTCT GGTGTGCCCT GGAGAGCATT CCCTGGGCCT ACGCAATCTT 720
CCAACTTAAG AATGCTCTGC AGACATCACT CTGGTTGCTC AAGGTGGGGC AGTAAACTTT 780
TATTTACAGG TCATCTGATA ACCCTGAACT CTAGCCCAAT GACCTGGAGA AGATGAAAGG 840
CAGCTGCATT GCTCAAGGTG AAAAAGAGAC ACAGGCTAGC AGAAAGACAC ACAGTGAATA 900
ACACCATCAA AGGAACGGAT GCATGGGAAG AGGAGAGATG GTGATGCCAG CCAGATGTGG 960
CCGTGGGCTG GTGTTTCCTC TGGCCAGCAG TTCCAATGAC ACCTCCTCCT GAGGGCTTTA 1020
CAGGGTGCCC AAATCGAACA ATGCCATACT CTGAGCTCCT TTCATACCTC TGTCCATTTT 1080
CAGAGGCTGC ACACATTACA AGGTTTTGGA ATTGATTTGT TTTTCTGCCC ACAGCAGCCT 1140
CCAGGCTCTC AGGGCATTGG AGCCTGTTCC TGGTACATCC TTCTACTCCA AATACCAAGT 1200
ACAGTGCTTG GAACATGGTG GCAGATCTTT AAAATTGTGT TTCTTTTCTT TTTTCTTTTT 1260
TTTTTTTTTT TTGAGACTGA ATCTCGCTCT GTTGCCTGGG CTGGAGTGCA GTGGCATGAT 1320
CTCGGCTCAC TGCAACCTCT GCCTCCTGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG 1380
AGTAGCTGGG ACTACCGGTG TGTACCACCA AGCCCAGCTA ATTTTTGTAT TTTTAGTAGT 1440
GACGGGGTTT CAGGCCTGAT AGGGACCCTC AGAATTGTCC TGCTGCAGGG CACAGATTCC 1500
CTGTATTCCT CAACTTCCCC ACCGCTCGAG GAGTTTCTCG AACTCCTGAC CTCGTGGTCC 1560
GCCCGCTTTG GTCTCCCAAA CTGCTGGGAT TACAGGCCTG AGCCACCGCG CCTGGCCTAA 1620
AATTGTATTT CATTGAGTGA AATCTGTTCC TAAGGAATTG CTTTCCAATG AGATAGTCCG 1680
GGCAGTCCTT TCTTCAGACT CTCCCTGACC CCATCACATA CGAGGCTTCC CTCTGACAAT 1740
GTCTGACTTC CCCTTGCTCC TGGAAGGAGC TGAGGGAGGG ACATCAATTC ATTATGACAC 1800
TGGCTTTTCT CAGCCTCTTG GAACCACGGG CCTACTTATG CCACCTCGGT GTTTCCCTGA 1860
GAAGATATGC TTGGGCTCAA CCTGTCTGCA CTCATTTCTA ACTCCCTTAG GCTTCCTTGT 1920
GTTGGGTAAG GCATTCTCCA TTTCGGTTGA ATTTTTTAAG TTTACTACTC AAAAGTATCA 1980
CTTATCAGGT CCCCAAATGG TCTAGGCAAA TACGTGTTCA CATTAGCCAC TGTCTTCTAG 2040
GAAAAATTCT CCTAAAGTAT TATTAAAAAT CTGCTCCTTG ATGAGTAATC ACTTGCTTTC 2100
TCTTTCCCCT TCTCGTCATT GTTTACTGTG CTCCGAATGT TTGCCAAAGG CGCAGGTGGG 2160
AGCCGTTCTG CGGCACGGGA GGCTTATTAT TCACGTGCAT TTCCACCGTG CAGTTGAGAA 2220
CTGATGATAT CACAGCAGTG ATATCTCTGT GGTTTCTATG AGCAGAACGG ATGGAAGCGA 2280
TACACCAGGC TCATCAAACC AGACCCAGGC AAATGCAGCC CTCAGGTCAT CACGCGCAGC 2340
TCTCTTCTGC TGGTGTCTGC AAAGCATTCT AAGAGCCTGG CTTGAAAATG CTTAAAAGCG 2400
CAAGGTGTAC GTTTTCAGAA CAAAATTAAT CCACCCAGTC TGCACAAACA GCTCCAAGAT 2460
CTTCTGCGGT ATAATTGACA TATAAGTCAC AATCATAAAA GTGAATCAGC CACGTCCCTG 2520
AAACACAGTC GGAGATGAGG TGCTAACTTC TTGAAGTGGC TGCATGAGTT TTCTTTGGCT 2580
GCTGTAACAA ACCATCACAT CAGTGGCTTA AACAACCCGA ATCTATTAAA AGTCCAACGC 2640
AGGTGTCGCT GAGCTAGAAT TGAGGTGTCA GCAGGCCTGT GTTCTTTCTG AAGAATGCAG 2700
GGGAGAAGCT GTTTCCTTAT CTTTTCCAGC TTCTAGGAAC CACCCATCTA TTTTGACTCG 2760
GGGCCCCTCT TCCACCTTCA AAGCCAGCGA TGGTGCCTTC CCCTGCCTTC CTTCCAGAGC 2820
CCTCTCTCCC TCTCCAGTTC TGCTGCCCTC TAATCCTTGT AGGATCCTTA 2870
|
