EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS052-38335 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr9:33150600-33152230 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1328899chr933151415hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:33150982-33151000GGAAGGAAATAAGTAAGG+6.5
EWSR1-FLI1MA0149.1chr9:33150978-33150996GGAAGGAAGGAAATAAGT+6.7
EWSR1-FLI1MA0149.1chr9:33150962-33150980GGATGGAAAGAAGGAAGG+7.73
EWSR1-FLI1MA0149.1chr9:33150974-33150992GGAAGGAAGGAAGGAAAT+9.03
EWSR1-FLI1MA0149.1chr9:33150970-33150988AGAAGGAAGGAAGGAAGG+9.09
EWSR1-FLI1MA0149.1chr9:33150966-33150984GGAAAGAAGGAAGGAAGG+9.47
Number of super-enhancer constituents: 35             
IDCoordinateTissue/cell
SE_00330chr9:33150154-33152533Adipose_Nuclei
SE_00992chr9:33150845-33151621Adrenal_Gland
SE_03080chr9:33150830-33151209Bladder
SE_09459chr9:33150683-33152077CD14
SE_10229chr9:33150691-33152191CD19_Primary
SE_10912chr9:33119344-33169982CD20
SE_19329chr9:33150695-33152114CD4p_CD25-_Il17p_PMAstim_Th17
SE_20045chr9:33150690-33152312CD56
SE_22416chr9:33150710-33152253CD8_primiary
SE_23687chr9:33150875-33151683Colon_Crypt_1
SE_26031chr9:33150287-33152385Duodenum_Smooth_Muscle
SE_26859chr9:33150779-33151670Esophagus
SE_27770chr9:33149455-33152321Fetal_Intestine
SE_28724chr9:33149325-33152320Fetal_Intestine_Large
SE_29800chr9:33150488-33152194Fetal_Muscle
SE_31534chr9:33150777-33151683Gastric
SE_34775chr9:33150487-33152230HeLa
SE_40894chr9:33150769-33152080Left_Ventricle
SE_41831chr9:33150862-33151334LNCaP
SE_42236chr9:33150804-33151823Lung
SE_44340chr9:33150635-33152125NHDF-Ad
SE_45447chr9:33150452-33151912NHLF
SE_45731chr9:33149399-33152178Osteoblasts
SE_46917chr9:33150883-33151589Ovary
SE_47814chr9:33151298-33151559Pancreas
SE_48426chr9:33150761-33152145Psoas_Muscle
SE_48738chr9:33150773-33151797Right_Atrium
SE_50176chr9:33150800-33151701Sigmoid_Colon
SE_51651chr9:33149245-33152315Skeletal_Muscle
SE_52621chr9:33150782-33151822Small_Intestine
SE_53402chr9:33150804-33151863Spleen
SE_56627chr9:33150139-33152742u87
SE_58985chr9:33124740-33168862Ly3
SE_62118chr9:33106994-33169093Toledo
SE_62346chr9:33106942-33169226Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93315093633151964
chr93315082833152043
Number: 1             
IDChromosomeStartEnd
GH09I033149chr93314900333152397
Enhancer Sequence
TACAAGAGGG ATTTTTTTGG GGTGATGGAA CTGTTCTGTA TCCTGATTGT GGTGGTAGAT 60
ACACAAAAAT ATGTATGTGT TAAAATTTAT AGACTATATG CCAAAAAGCC AATTTTATTG 120
TAGGTTAATC TAAAAAAATT TTTTTTAAAG TTAAGAATAC ATCTATGTAT AAAGCAGTGG 180
CTTCCATTTT GGCAAGAGCA AAAACAGATA CACAAACTAT AAATACGTTA GAATAGTTGC 240
CTGTGATATA CCTGGGAAAT AGAAGTGGGA ATGAGGACAA AATAAAACAA ATACATGAGG 300
CAAGAGAGTC CATGAGTAGA CCCCAATGAT GATTATTGGC CATGAAAGGA AGCTTGATGG 360
CTGGATGGAA AGAAGGAAGG AAGGAAGGAA ATAAGTAAGG GAGAGATGGC GGATGGAGCT 420
GGATGTGTCC TTCCAGGGCT GTACAAAGGA GGGGGACCCC AACCCCTAGT CCAGACAAAG 480
GTCCCTAAGG CAGGTGTACA GTATTGTGGG GATGAATTCA TCAGCCACGA GAGACTGACC 540
CATCTAATGT TAAATTCACT TCCCTGCTCT GACTGCTGAC TCACCAGCAG TTAGCTTATC 600
CTGCGGCTTC CCTTGCAGTG AATTCAGCCA GAGATTTCTA AGCTACTCAA TAACAGTTCT 660
AATCTTCCCA GTAAAGCTGC AACTTTGCAT TCCAGTATGT AAGTAAGTCT CCTGGGAGTT 720
TTATTACTGA GTCAGCTGCC CCTCTAATCA GTTTTGGAGC CCCAGCAGAT TTTCTGGAGC 780
TGCGGTGCTG ACTACGAGCA CATCCTTCTC TCTCCACCTA GAACCAGACC TTGGACTGTG 840
GAGGGCCCAC TACTCCTATG GGCCATCTGG GCACTCAGCC AGCCAAGTAC TCCTGGCAAT 900
ATCTCTCTGG TGTCAGGACT ACTTTAAATG TAGCCAGCTC CAATTTCCTT CTCTAAGGAG 960
TGGGGATAAT TATGCCTTCC TTTCAGATGT AAGTGAAATA ATACATATAC ATACTTATCG 1020
CATGTTCTTA TTGAGCTAAT AGATGTTCAA TAAATGTTAC TTTCCCTTCT CCCCTGACTC 1080
CTTAGAACTT CAGAGCTTAC AAATTACTAC AGCTCTATCA GCACACATGG CTAAATTTTC 1140
ACATTTCTAC TCTTAGCCAC TAGAATCACT GATAGATTTG GAGGAAAACT CTGGGACCTT 1200
AAAGGGTCCC TGGAGTATTA CATAAAGCTT CTTGCAGCAT GAGAGTTGAA CAGAAATTCT 1260
GTTCATCTTT TGCTGTCGAA GCCAAGTTGG TGGCTTCTAA AGAACCAACT TAGAAGAAAA 1320
CTCAGGAGAA AAATTTTATC ATTTTGGGAT GGTGAAGACC TGCTTAAGTA TGAAAGCAAC 1380
CTGAAGTCAT AAAGGAAAAC ATAGATTTAA ACACATAAAA ATTCAAAACT TCTGGCCGAG 1440
TGCAGTGGCT CACGCCTGTA ACCCCAGCAC TTTGGGAGGA TCATTTGAGA TCAGGAGTTT 1500
GAGATCAGCT TGACCTACAT AGTGAAACCC CGTCTCTACT AAAACACAAA AATTAGCTGG 1560
GTGTGGTGGC GGGTGCCTGT AATCACAGCT TCTCGGGAAG CTGAGGCAGG AGAATCGCTT 1620
GAACCCAGGA 1630