EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS073-13045 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr7:44661870-44663170 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXF2MA0030.1chr7:44662014-44662028CTTGTTTACCTTTA-6.96
Lhx3MA0135.1chr7:44663131-44663144AAATTAATTAATC+7.82
POU6F1MA0628.1chr7:44663133-44663143ATTAATTAAT+6.02
POU6F1MA0628.1chr7:44663133-44663143ATTAATTAAT-6.02
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_09293chr7:44656533-44664867CD14
SE_12002chr7:44661970-44664769CD3
SE_14587chr7:44661595-44666552CD4_Memory_Primary_7pool
SE_15490chr7:44662284-44664805CD4_Memory_Primary_8pool
SE_16434chr7:44661773-44664498CD4_Naive_Primary_8pool
SE_16951chr7:44661854-44664820CD4p_CD225int_CD127p_Tmem
SE_17851chr7:44660970-44667023CD4p_CD25-_CD45ROp_Memory
SE_18656chr7:44661057-44666341CD4p_CD25-_Il17-_PMAstim_Th
SE_19294chr7:44661232-44666908CD4p_CD25-_Il17p_PMAstim_Th17
SE_20655chr7:44662135-44663196CD56
SE_21218chr7:44661809-44663212CD8_Memory_7pool
SE_22840chr7:44661619-44664737CD8_primiary
SE_24636chr7:44662278-44662951Colon_Crypt_2
SE_26120chr7:44660088-44663486Duodenum_Smooth_Muscle
SE_27427chr7:44661906-44662995Esophagus
SE_27654chr7:44653619-44664659Fetal_Intestine
SE_28557chr7:44653546-44666729Fetal_Intestine_Large
SE_32407chr7:44662061-44663077Gastric
SE_34691chr7:44659818-44663107HeLa
SE_37328chr7:44659783-44663176HSMMtube
SE_40682chr7:44661832-44663053Left_Ventricle
SE_42075chr7:44662099-44663009LNCaP
SE_42544chr7:44660490-44663115Lung
SE_43768chr7:44661678-44664721MM1S
SE_46384chr7:44661325-44663119Osteoblasts
SE_48519chr7:44661882-44663185Psoas_Muscle
SE_50531chr7:44661881-44663149Sigmoid_Colon
SE_52560chr7:44661291-44663148Small_Intestine
SE_53907chr7:44660114-44664683Spleen
SE_62947chr7:44653723-44680812Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr74466282444662939
chr74466204844662924
Number: 1             
IDChromosomeStartEnd
GH07I044613chr74465347244666508
Enhancer Sequence
TGTCTTCCTT AAATATATCA GTGGAAAAAC TTGGAGTGTA GTTGGAGGTA GGAAGAACTA 60
CCGAATTAAC TTAAAACTTT TGATTTCTAA AGTGAAAACC CAGGGGTAAA GATTGCATTC 120
CCTAATTATA TCCAGAATAT ATTGCTTGTT TACCTTTAAT TTGTAAGGAG CAAGTTTTTG 180
TTTGTTGTTC AGTTTGTTTT TAAAGAATAT GTTCTGCTGT TTACTTTTGC TGACCTATCT 240
CTTCTCAGTG GAGCAGGCCA GAGGTGAATG CAGGACACTC TAAGCCCTCT CTCTTGGTGT 300
CCCTTAAGTG TATTCTGAGC ATATTTGGGC CAAGAGGAAG TTTCTGATAA ATAATATAGA 360
AGATATTTTT ATGTAACAGT TATTTCTGGG TAATTCACAC TATGTTTCAG AGCTTGGATT 420
TTCTTCGGGT AGGTGTGGAC ATGGAGTGTA GTTCTAACTT TACAACCAGA GCACCTGCTT 480
TGAGACAAAT TCATGAGCAA CCATGTAGGC CAGCAAGCAC CTTTTTTTCC ACAGGCAGCG 540
TCCTTGTGAA CTTTCCGCTT GGATCCTGAC TCTGCTGTTA GTAGCCTATG ACCTTGGATG 600
AAATGTAAGG GAATAGAAAC TGAAGCTATC TGTAAAGTGA AAGAGCTGGT GCCTGCCTTA 660
TTGGGAGCCT CTGGGTTTAT GTATGAGTCA GATGCGTAGA GTTGCTCACC ATGGAGGGCC 720
CAGGGTAGGC AGGCATTATT GAACAACTGC TCCATGTGCT CTTTTCAATC TTTGCAGACC 780
CCACCCACGT CTCCCTTGCT CAGACCTGGC TCCCCATGGC TTATGAAAGG GGGCTGAGTG 840
CAGAAGGTGG CAGGCAGGAC ACTGGACAAC CCTCTGTGGC TTTTCCTTAC CCTTCGTAGT 900
ACCATGAGAT TCTGGCTCTT CCCGTCTCTG TGTTTCTGCC TATGGGTCCT TCCACATGCA 960
GTGCCTCGTC TTCCCTCCTT CCCATCCATG TCCTTTTGTC TTCAGGCACA CCCACTTGGA 1020
AGGAGCCCAT CCTCTCACAG GGTCTGCTGG CATATTCTGC ACCTCTCAAG TACTCATATT 1080
TCCTCTGCAA TCTTTTCTAT GTTGTTTTTC CTCTGCTCAA GGGTAAATTG AGAGTAAGGA 1140
AAGTATTTTT CTAATTTCTT TGTATTTTCC ATAATATTGT AAGTACAGCA GGTACTCAGT 1200
AGTTTCTGGA CAGATTAGAA AATGTTTTAC TTATTCTCCA ATTAATCCTA ATCCTAATTC 1260
TAAATTAATT AATCCTTGTT GCCTTTCTTC TAATTGTTTT 1300