EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS116-28883 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr6:7137020-7138330 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MIXL1MA0662.1chr6:7138275-7138285GTTAATTAGA-6.02
PLAG1MA0163.1chr6:7137493-7137507CCCCCCTGAGCCCC-6.3
ZNF263MA0528.1chr6:7138015-7138036TCCTCTTCCTCTCCCTGCCCT-6.73
Number of super-enhancer constituents: 42             
IDCoordinateTissue/cell
SE_00099chr6:7123924-7150008Adipose_Nuclei
SE_01064chr6:7137109-7138270Adrenal_Gland
SE_09175chr6:7135375-7139462CD14
SE_11591chr6:7133887-7142531CD20
SE_12764chr6:7137643-7137788CD34_fetal
SE_13205chr6:7137388-7138448CD34_Primary_RO01480
SE_13456chr6:7135929-7142480CD34_Primary_RO01536
SE_14595chr6:7135831-7148942CD4_Memory_Primary_7pool
SE_19023chr6:7135013-7140192CD4p_CD25-_Il17-_PMAstim_Th
SE_20929chr6:7137036-7139118CD8_Memory_7pool
SE_23267chr6:7137095-7138233Colon_Crypt_1
SE_24175chr6:7137141-7138108Colon_Crypt_2
SE_26179chr6:7136637-7142427Duodenum_Smooth_Muscle
SE_26569chr6:7136972-7138795Esophagus
SE_28374chr6:7136657-7148734Fetal_Intestine
SE_29027chr6:7136477-7148714Fetal_Intestine_Large
SE_30159chr6:7136894-7139231Fetal_Muscle
SE_31247chr6:7134204-7139846Fetal_Thymus
SE_31471chr6:7136965-7138779Gastric
SE_32706chr6:7135036-7139613GM12878
SE_37264chr6:7136836-7139374HSMMtube
SE_39870chr6:7136923-7138909K562
SE_41219chr6:7137060-7138874Left_Ventricle
SE_42377chr6:7136857-7138448Lung
SE_43730chr6:7135022-7140058MM1S
SE_45215chr6:7136844-7138806NHLF
SE_46025chr6:7136854-7139706Osteoblasts
SE_48011chr6:7137165-7137728Pancreas
SE_48011chr6:7137772-7138188Pancreas
SE_48253chr6:7136749-7138865Psoas_Muscle
SE_50177chr6:7136950-7138799Sigmoid_Colon
SE_51588chr6:7136806-7143938Skeletal_Muscle
SE_51921chr6:7137298-7138553Skeletal_Muscle_Myoblast
SE_52972chr6:7136514-7138842Small_Intestine
SE_53741chr6:7136950-7138836Spleen
SE_54903chr6:7137316-7139996Stomach_Smooth_Muscle
SE_55541chr6:7136986-7138622Thymus
SE_59725chr6:7099938-7157593Ly4
SE_63714chr6:7137237-7139122HSMM
SE_64591chr6:7136710-7139896NHEK
SE_65660chr6:7136784-7138592Pancreatic_islets
SE_66826chr6:7137085-7139202Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr671379667138068
Number: 1             
IDChromosomeStartEnd
GH06I007134chr671350157149832
Enhancer Sequence
TGTTTTCAAG AGTTCTTTAT TATCAGGTGG CTTGTGAAAG CCCGTCGTTA ACCAAACGTG 60
TTGTGTTTGC CTCAGAATTT TATTAAAAAG GTATGCATAG GTTCATATCC CCCTTATGTG 120
AGGTGGCAGT GAAACAGAAA CTTGATAGAA ATATTGAGGA GGGGAAAAGA TGAAGCCACC 180
GCGGCACCTG GCCTCCCTCT TTCACTTCCC TTTCCAACTC TGCTCCTTTG AGATGTTCTT 240
CGAGAAGATG GAGGAAGCTT GCTGGGTTTA GGGTCATCAC CCAGGATCTG GCGACGGGAG 300
TGCCTCAACA TGGGGAGTTC CCTCCCCAAA GCCCAGAGCT AATTCGTCAC ATCCAGCTGC 360
TGTCAGGAGT TGAGCAGTCC TGTCCCCTGG CTTTCCTGGG AAGGCCTGGG TGGAGGCGGC 420
AGGAGCAGGC AAGGGACCAA GAGAGTGCCT GCTAGACCTG ATGCCTCTCC CTTCCCCCCT 480
GAGCCCCCAG GGAAGGAGCT GCCTTATAGA CTCGGGTACA GGGAGGCAGG GAATAGAGGG 540
TTGGAATCCA GAAAAGAGGG TGGAGGGCAT GACTGCAGTT ACTGCCATTG TCTCAGGACA 600
GACAGACCAA GCCCTGGTAC AGAAATTGTT TGGCTGTTGG CCTTTTCTCT TCAGATGTTT 660
ACATGCAGGA AGTGCCTTTG ATAAAGTATG GTTTGCTAAC ATGAGTATGA TATGCATGCG 720
CATTTTTGGA TGCCAAACAC ATAGGCAGAT GAAACTAAGA AGCCAGATGC TAAGATAGTT 780
GTTGATGAAT TGAAACTAGC CTAACTGGCT CCACTGTTGG AGTCATTTGC TCAAACTACT 840
CCAAACTTTT GTTTGGTCTA CTGAAAACAT TAGTTGGAAA GGTACAGCGT TAATTTAAGG 900
CAGGGAAGCC TCCAGCACGT GAGAGTCGTG TCTCTCTCGG TGATGCTGGG AGGGAAGGAT 960
GGGAGATGAG AGTCATTTCA CGGCCGCCTA GCTCCTCCTC TTCCTCTCCC TGCCCTGGAG 1020
CTGCAGCCTC AGCTTTCAGA GTCTCTTGCC TGGTGGTAGG CCCGGCGAGC GGTTGGATTT 1080
TAAGTATCTC AGTTATTTTC AGTATCATCA GTCATCACTT TCAGAGTTCC TTTTCTTTTT 1140
CAAGGGTACC CAGTCTAACT GTTTAGCTCC TTTTCAATAG CCCTCCTCAC TCACTTACGC 1200
CTAGTCAGGA AGATTAATAA TGTTAACTGA TTTACTATCA CTGCAAAAAG CATTAGTTAA 1260
TTAGACTTTT ACACCTCAGT CAGATGGCAT TAGACACCCT TTGTGCACTT 1310