| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13493 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:85145590-85148130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr2:85147161-85147172 | GATGAGTCACA | - | 6.14 | | Foxd3 | MA0041.1 | chr2:85147247-85147259 | GATTGTTTATTT | + | 6.62 | | HNF4G | MA0484.1 | chr2:85147639-85147654 | TGGCCTTTGGCCTTG | - | 6.47 | | HNF4G | MA0484.1 | chr2:85147595-85147610 | TGGCCTTTGGACTCT | - | 7.58 | | JUN(var.2) | MA0489.1 | chr2:85147162-85147176 | ATGAGTCACATCCT | - | 6.21 | | JUND | MA0491.1 | chr2:85147161-85147172 | GATGAGTCACA | - | 6.14 | | Nr5a2 | MA0505.1 | chr2:85147876-85147891 | GCTGGCCTTGAACTC | - | 8.25 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_10467 | chr2:85145440-85148104 | CD19_Primary | | SE_14858 | chr2:85146216-85148097 | CD4_Memory_Primary_7pool | | SE_15828 | chr2:85146211-85147858 | CD4_Naive_Primary_7pool | | SE_17329 | chr2:85144702-85148021 | CD4p_CD25-_CD45RAp_Naive | | SE_18307 | chr2:85145257-85148272 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19290 | chr2:85146834-85148007 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22056 | chr2:85146279-85147703 | CD8_Naive_8pool | | SE_24195 | chr2:85147396-85147781 | Colon_Crypt_2 | | SE_27502 | chr2:85146415-85148139 | Esophagus | | SE_32545 | chr2:85146405-85147995 | GM12878 | | SE_34685 | chr2:85144533-85148900 | HeLa | | SE_35873 | chr2:85145245-85148284 | HMEC | | SE_37561 | chr2:85145355-85148665 | HSMMtube | | SE_39196 | chr2:85146289-85148051 | IMR90 | | SE_43289 | chr2:85146287-85148018 | Lung | | SE_45342 | chr2:85146235-85148013 | NHLF | | SE_47378 | chr2:85146394-85148070 | Panc1 | | SE_50337 | chr2:85146275-85148041 | Sigmoid_Colon | | SE_52528 | chr2:85146343-85148031 | Small_Intestine | | SE_54030 | chr2:85146413-85147977 | Spleen | | SE_55507 | chr2:85147282-85147950 | Thymus | | SE_55909 | chr2:85145260-85146133 | u87 | | SE_55909 | chr2:85146272-85148271 | u87 | | SE_57573 | chr2:85146370-85147966 | VACO_503 | | SE_58212 | chr2:85146543-85147124 | VACO_9m | | SE_58212 | chr2:85147243-85147947 | VACO_9m | | SE_65145 | chr2:85146145-85148023 | NHEK | | SE_67823 | chr2:85145260-85146133 | u87 | | SE_67823 | chr2:85146272-85148271 | u87 |
|
| | 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 |
| GH02I084918 | chr2 | 85145334 | 85148597 |
|
Enhancer Sequence | TTTGACCAAA TAGCTGACAC CATAGCCAAG TTCACACATA AAATTAACCA TCACACTGTT 60
TGAGGTTTTT TTTTTTTTTT TCCATTTCAT CTGCACAGGC ACCTGGCTTC TAGCAGACAT 120
TTTCTCCTTG GATCTGGGCA CCAGTACATC CCATGCCAGG CCTGGCCCAC CACAAGGACC 180
ACTGAATGCA GAAGCCCAGC TCCCACTCCC ACCCAGGGCC ACGAAATGAC ACTAGGGATG 240
GAAACTGATG TAGGATGGTG CAGCAGAAAG CATTAAGGTG ACTGGGATCT CAGAGTTGCT 300
ATACCAGGCG TGGACTACTC CTTCCAGACA TCTTTAATCT TTATCAGGAA GATGAATAAG 360
CTTCTATTAT GATATATAAG TCACTGGGTT TTTGTTTGTT TTTGTTTTCT TTTTTTGTTT 420
TGTTTTGTTT TTGTTTTGAG ACGGAGTCTC TCTGTCACCC AGATTAGAGT GCAATGGTAC 480
CATCTCAGCT CACTGCAACC TCCCCCTCCT GGGTTCAAGC GATTCTCCCA CCTCAGATTC 540
CAAAGTAGCT GGGATTACAG GCACCTGCCA TCATGCCCAG CTAATTTCTG TATTTTTGTA 600
GAGATGGGGT TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTG AGGTGATCCG 660
CCTGCCTCAG CCTCCCAAGG TGCTGGGATT ACAAGCGTGA GCCACCACGC CTGGTCGTGT 720
TTTTGTTTCC TGAGACAGAG TCTCACTCTG TCACCCAGGC TGGAGTGCAG TGGTGCCATC 780
TCGACTCACT GCAACCTCCG CCTCCCAGGT TCAAGTAATT CTCCTGCATC AGCCTCCGGA 840
GTAGCTGGGA CTACAGGTAC TGCGCCACTA TGCCCGGCTA ATTTTTGTAT TTTTAGTAGA 900
GATGGGGTTT CACCATGTTG GCCAGCCTGG TCTCAAACTC CTGACCTCAG GTAATCCATC 960
CGCCTTGGCC TCCCAAAGTG CTGAGATTAC AGGCGTGGGC CACCATGCCT GGCCAGACAG 1020
TCCAATATTT TTAAATCAGC CATAAATCTA TGCACCGAAT AATGTCTCTC TCTCTCTCTC 1080
TGACACATAC ACACATACAC ACATGCGCAC GCGTGCACAC CCACACATTG TTACCACTTA 1140
GAAGAGTGCC AGGCCCAGAT GGTTTCACAG ACGATTGCTT TCAAAGCTGC AAGAAAGCAA 1200
TAACTTCAAT ACCTCAAAAT TTGTTTCAGT AGTTAGAAAA GGACATATGC TTCCTGTGAT 1260
GGTTAATTTT AGCTGTCAAC TTGACTTGAT TAAGTAATAC ACTAGTCTCC CCTTATCCAT 1320
GGAGGGTATG TTCCAAGATC CCCAGTGGAT GCCTGAAGCC ACACATGTAC CGAACCCTGT 1380
ACACACCTAT GATAACGTTT AATTTATAAA TTAGGCACAG TAAGAGATTA ACAACTAATA 1440
ATAAAATAGA ACAATTAAAC AGTTGAACAC AAGCACTGTG ATGCTGTGAC AGTCACTCGT 1500
AACTGAGATG GCTGCTAAGA GACTAGCTAA CGGGTGAGTA GTGTATACAA CGTGGAAACA 1560
CTGGACAAAG GGATGAGTCA CATCCTGGGA GGGACAGAGT GGAATGCCAT GAGATTTCAT 1620
CATGTTACAC AGAACGATGA GCCATTTAAA ACTTACGGAT TGTTTATTTC TGGAATTTTT 1680
AATTTAATAT TTTCAGACCA AGGTTGACCA GGAGTAACTA AAACTACAGA AAGCAAAACT 1740
GAATAAAGTG GGGAGTCGAG AACCTAGAGA GCTGGTAAAG CATTCTTTCT AGGTGTGTCT 1800
GTGAGGGTGT TTTCACAGGA GATTGGCATG TGAGTGGGTG GGCTGACTGA GGAAGATCTG 1860
CCCTCAGTGT GGGCGGACAA CATCCAATTG GCTGTGGGCC CAGATAGAAC CAAAAGGCAG 1920
AGAAAAGGCA AATTCTTTTT TTCTCTCTCC TGAAGCTGGG CCATCCTTCT TCTTCTGACC 1980
TTGGACATCA GAACTGCAGG CTCCCTGGCC TTTGGACTCT GGGTCTTACA TTAGCAGCCC 2040
CCAGGTTCTT GGCCTTTGGC CTTGGACTGA GAATTACACT ATCAGCTGCC CTGGTTCTGA 2100
GACTTTAGGA CTTGAACTGA GCCCCACTGT GGTATTCCAC GGTCTCCAGC TTACAGACAG 2160
TCTGTCGTGG GACTTTTCAC CTCCCTAATC TCATGAGCCA ATTCCCCTAA TAAATCCCCT 2220
CTCATATATC TATATACAGT CGCCCCTCAT ATCTATGGGA GATGGGTTCC AGGTTATGTT 2280
GCCCAGGCTG GCCTTGAACT CTTGGGCTCA AGCTATCCTC CCATCTCAGC TTCCCAAGTA 2340
GCTAGGACTA TCATATTCTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC GCTCTGTCAC 2400
CCAGGCTGGA GTGCAGTGGT GCGATCTCGG CTCACTGCAA GCTCTGCCTC CCGGGTTCAT 2460
GCCATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGACTAC AGGCGCCCAC CACCACACCC 2520
AGCTAATTTT TTTTTTTTTT 2540
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